Canonical Allele Identifier: CA402699996
Gene: RTTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.70196630T>G , CM000680.2:g.70196630T>G GRCh38
NC_000018.9:g.67863866T>G , CM000680.1:g.67863866T>G GRCh37
NC_000018.8:g.66014846T>G NCBI36
NG_033104.1:g.14097A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000255674.11:c.712A>C ENSP00000255674.7:p.Lys238Gln
ENST00000638251.1:c.712A>C ENSP00000491968.1:p.Lys238Gln
ENST00000640376.1:c.193A>C ENSP00000491654.1:p.Lys65Gln
ENST00000640654.1:n.262A>C
ENST00000640736.1:n.560A>C
ENST00000640769.2:c.712A>C MANE Select ENSP00000491507.1:p.Lys238Gln
ENST00000255674.10:c.712A>C ENSP00000255674.6:p.Lys238Gln
ENST00000581161.5:c.712A>C ENSP00000462926.1:p.Lys238Gln
ENST00000581583.1:n.780A>C
ENST00000583043.5:c.82A>C ENSP00000462733.1:p.Lys28Gln
NM_173630.3:c.712A>C NP_775901.3:p.Lys238Gln
XM_005266679.1:c.-1842A>C XP_005266736.1:n.-1842A>C
XM_006722434.2:c.712A>C XP_006722497.1:p.Lys238Gln
XM_006722435.2:c.712A>C XP_006722498.1:p.Lys238Gln
XM_011525902.1:c.712A>C XP_011524204.1:p.Lys238Gln
XM_011525903.1:c.712A>C XP_011524205.1:p.Lys238Gln
XM_011525904.1:c.712A>C XP_011524206.1:p.Lys238Gln
XM_011525905.1:c.712A>C XP_011524207.1:p.Lys238Gln
XM_011525907.1:c.712A>C XP_011524209.1:p.Lys238Gln
XM_011525908.1:c.712A>C XP_011524210.1:p.Lys238Gln
XR_430072.2:n.750A>C
XR_935213.1:n.750A>C
NM_001318520.1:c.-1842A>C NP_001305449.1:n.-1842A>C
XM_006722434.3:c.712A>C XP_006722497.1:p.Lys238Gln
XM_006722435.3:c.712A>C XP_006722498.1:p.Lys238Gln
XM_011525902.2:c.712A>C XP_011524204.1:p.Lys238Gln
XM_011525903.2:c.712A>C XP_011524205.1:p.Lys238Gln
XM_011525904.3:c.712A>C XP_011524206.1:p.Lys238Gln
XM_011525905.2:c.712A>C XP_011524207.1:p.Lys238Gln
XM_011525907.2:c.712A>C XP_011524209.1:p.Lys238Gln
XM_011525908.3:c.712A>C XP_011524210.1:p.Lys238Gln
XM_017025693.1:c.712A>C XP_016881182.1:p.Lys238Gln
XM_017025694.1:c.70A>C XP_016881183.1:p.Lys24Gln
XM_017025696.1:c.-1460A>C XP_016881185.1:n.-1460A>C
XM_024451139.1:c.-69A>C XP_024306907.1:n.-69A>C
XM_024451140.1:c.-69A>C XP_024306908.1:n.-69A>C
XR_430072.3:n.780A>C
XR_935213.2:n.780A>C
NM_001318520.2:c.-1842A>C NP_001305449.1:n.-1842A>C
NM_173630.4:c.712A>C MANE Select NP_775901.3:p.Lys238Gln