Canonical Allele Identifier: CA1644571229
Gene: RARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87518708T= , CM000668.2:g.87518708T= GRCh38
NC_000006.11:g.88228426T= , CM000668.1:g.88228426T= GRCh37
NC_000006.10:g.88285145T= NCBI36
NG_008601.1:g.76310A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000451155.2:c.812A= ENSP00000389656.2:p.Lys271=
ENST00000493269.2:n.1357A=
ENST00000497828.2:n.3532A=
ENST00000684790.1:c.*343A= ENSP00000509974.1:n.*343A=
ENST00000685069.1:c.398A= ENSP00000509876.1:p.Lys133=
ENST00000685219.1:n.1373A=
ENST00000685336.1:c.*760A= ENSP00000508757.1:n.*760A=
ENST00000685376.1:c.*459A= ENSP00000508661.1:n.*459A=
ENST00000685408.1:c.812A= ENSP00000509026.1:p.Lys271=
ENST00000685701.1:c.398A= ENSP00000509573.1:p.Lys133=
ENST00000685881.1:c.812A= ENSP00000510572.1:p.Lys271=
ENST00000686142.1:c.812A= ENSP00000510793.1:p.Lys271=
ENST00000686154.1:c.398A= ENSP00000508436.1:p.Lys133=
ENST00000686196.1:n.1582A=
ENST00000686284.1:c.398A= ENSP00000510099.1:p.Lys133=
ENST00000686371.1:n.839A=
ENST00000686407.1:c.398A= ENSP00000509880.1:p.Lys133=
ENST00000686857.1:c.*253A= ENSP00000509934.1:n.*253A=
ENST00000686988.1:c.1435A= ENSP00000508830.1:n.1435A=
ENST00000687090.1:n.1702A=
ENST00000687437.1:c.1337A= ENSP00000508968.1:p.Lys446=
ENST00000687579.1:c.*383A= ENSP00000510257.1:n.*383A=
ENST00000687586.1:c.260A= ENSP00000508441.1:p.Lys87=
ENST00000687729.1:c.781-26A= ENSP00000508582.1:n.781-26A=
ENST00000687909.1:c.*747A= ENSP00000508659.1:n.*747A=
ENST00000688106.1:c.398A= ENSP00000509529.1:p.Lys133=
ENST00000688391.1:n.1845A=
ENST00000688532.1:c.260A= ENSP00000510320.1:p.Lys87=
ENST00000688808.1:n.1843A=
ENST00000688842.1:n.3811A=
ENST00000689174.1:c.812A= ENSP00000510542.1:p.Lys271=
ENST00000689206.1:c.398A= ENSP00000510495.1:p.Lys133=
ENST00000689561.1:n.2353A=
ENST00000689594.1:n.2329A=
ENST00000689952.1:c.*675A= ENSP00000508977.1:n.*675A=
ENST00000690205.1:c.*1215A= ENSP00000508972.1:n.*1215A=
ENST00000690622.1:c.398A= ENSP00000508528.1:p.Lys133=
ENST00000690705.1:c.*253A= ENSP00000509923.1:n.*253A=
ENST00000690884.1:c.*253A= ENSP00000509931.1:n.*253A=
ENST00000691205.1:n.2303A=
ENST00000691238.1:c.*459A= ENSP00000510094.1:n.*459A=
ENST00000691533.1:n.1373A=
ENST00000691634.1:n.1218A=
ENST00000691725.1:c.1337A= ENSP00000509453.1:p.Lys446=
ENST00000691815.1:c.*253A= ENSP00000509579.1:n.*253A=
ENST00000692270.1:c.*253A= ENSP00000510055.1:n.*253A=
ENST00000692394.1:c.116A= ENSP00000509567.1:p.Lys39=
ENST00000692684.1:c.812A= ENSP00000509712.1:p.Lys271=
ENST00000692843.1:c.*324A= ENSP00000509592.1:n.*324A=
ENST00000693327.1:c.812A= ENSP00000509195.1:p.Lys271=
ENST00000693431.1:c.812A= ENSP00000509147.1:p.Lys271=
ENST00000693605.1:c.*253A= ENSP00000510050.1:n.*253A=
ENST00000369536.10:c.1337A= MANE Select ENSP00000358549.5:p.Lys446=
ENST00000369536.9:c.1337A= ENSP00000358549.5:p.Lys446=
ENST00000497828.1:n.440A=
NM_020320.3:c.1337A= NP_064716.2:p.Lys446=
XM_005248735.3:c.812A= XP_005248792.2:p.Lys271=
XM_005248736.3:c.812A= XP_005248793.2:p.Lys271=
XM_005248737.3:c.812A= XP_005248794.2:p.Lys271=
XM_011535947.1:c.1337A= XP_011534249.1:p.Lys446=
XM_011535948.1:c.1337A= XP_011534250.1:p.Lys446=
XM_011535949.1:c.1337A= XP_011534251.1:p.Lys446=
XM_011535950.1:c.812A= XP_011534252.1:p.Lys271=
XM_011535951.1:c.812A= XP_011534253.1:p.Lys271=
XM_011535952.1:c.398A= XP_011534254.1:p.Lys133=
XM_011535953.1:c.398A= XP_011534255.1:p.Lys133=
XM_011535954.1:c.398A= XP_011534256.1:p.Lys133=
XM_011535955.1:c.398A= XP_011534257.1:p.Lys133=
XR_241848.1:n.1393A=
NM_001318785.1:c.812A= NP_001305714.1:p.Lys271=
NM_001350505.1:c.1337A= NP_001337434.1:p.Lys446=
NM_001350506.1:c.812A= NP_001337435.1:p.Lys271=
NM_001350507.1:c.812A= NP_001337436.1:p.Lys271=
NM_001350508.1:c.812A= NP_001337437.1:p.Lys271=
NM_001350509.1:c.812A= NP_001337438.1:p.Lys271=
NM_001350510.1:c.812A= NP_001337439.1:p.Lys271=
NM_001350511.1:c.812A= NP_001337440.1:p.Lys271=
NM_020320.4:c.1337A= NP_064716.2:p.Lys446=
NR_134857.1:n.1408A=
NR_146738.1:n.1680A=
NR_146739.1:n.1489A=
NR_146740.1:n.1757A=
NR_146741.1:n.1419A=
NR_146742.1:n.1791A=
NR_146743.1:n.1629A=
NR_146744.1:n.1757A=
NR_146745.1:n.1416A=
NR_146746.1:n.1851A=
NR_146747.1:n.1195A=
NR_146748.1:n.1655A=
NR_146749.1:n.1629A=
NR_146750.1:n.1753A=
NR_146751.1:n.1633A=
NR_146752.1:n.1697A=
NR_146753.1:n.1549A=
NR_146754.1:n.1493A=
NR_146755.1:n.1757A=
NR_146756.1:n.1412A=
NR_146757.1:n.1683A=
NR_146758.1:n.1412A=
NR_146759.1:n.1412A=
XM_011535949.3:c.1337A= XP_011534251.1:p.Lys446=
XM_017011073.1:c.812A= XP_016866562.1:p.Lys271=
XM_017011074.2:c.812A= XP_016866563.1:p.Lys271=
XM_017011075.2:c.812A= XP_016866564.1:p.Lys271=
XM_017011076.2:c.812A= XP_016866565.1:p.Lys271=
XM_017011077.2:c.812A= XP_016866566.1:p.Lys271=
XM_017011078.2:c.812A= XP_016866567.1:p.Lys271=
XM_024446494.1:c.812A= XP_024302262.1:p.Lys271=
NM_020320.5:c.1337A= MANE Select NP_064716.2:p.Lys446=
NM_001318785.2:c.812A= NP_001305714.1:p.Lys271=
NM_001350505.2:c.1337A= NP_001337434.1:p.Lys446=
NM_001350506.2:c.812A= NP_001337435.1:p.Lys271=
NM_001350507.2:c.812A= NP_001337436.1:p.Lys271=
NM_001350508.2:c.812A= NP_001337437.1:p.Lys271=
NM_001350509.2:c.812A= NP_001337438.1:p.Lys271=
NM_001350510.2:c.812A= NP_001337439.1:p.Lys271=
NM_001350511.2:c.812A= NP_001337440.1:p.Lys271=
NR_134857.2:n.1363A=
NR_146738.2:n.1635A=
NR_146739.2:n.1444A=
NR_146740.2:n.1712A=
NR_146741.2:n.1374A=
NR_146742.2:n.1746A=
NR_146743.2:n.1584A=
NR_146744.2:n.1712A=
NR_146745.2:n.1371A=
NR_146746.2:n.1806A=
NR_146747.2:n.1150A=
NR_146748.2:n.1610A=
NR_146749.2:n.1584A=
NR_146750.2:n.1708A=
NR_146751.2:n.1588A=
NR_146752.2:n.1652A=
NR_146753.2:n.1504A=
NR_146754.2:n.1448A=
NR_146755.2:n.1712A=
NR_146756.2:n.1367A=
NR_146757.2:n.1638A=
NR_146758.2:n.1367A=
NR_146759.2:n.1367A=