Canonical Allele Identifier: CA341436682
Gene: WARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119033236T>C , CM000663.2:g.119033236T>C GRCh38
NC_000001.10:g.119575859T>C , CM000663.1:g.119575859T>C GRCh37
NC_000001.9:g.119377382T>C NCBI36
NG_050658.1:g.112553A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235521.5:c.758A>G MANE Select ENSP00000235521.4:p.Lys253Arg
ENST00000235521.4:c.758A>G ENSP00000235521.4:p.Lys253Arg
ENST00000369426.9:c.*124A>G ENSP00000358434.5:n.*124A>G
NM_015836.3:c.758A>G NP_056651.1:p.Lys253Arg
NM_201263.2:c.*124A>G NP_957715.1:n.*124A>G
XM_005270350.2:c.704A>G XP_005270407.1:p.Lys235Arg
XM_006710283.1:c.476A>G XP_006710346.1:p.Lys159Arg
XM_011540493.1:c.689A>G XP_011538795.1:p.Lys230Arg
XM_011540494.1:c.689A>G XP_011538796.1:p.Lys230Arg
XM_011540495.1:c.500A>G XP_011538797.1:p.Lys167Arg
XM_005270350.3:c.704A>G XP_005270407.1:p.Lys235Arg
XM_011540494.2:c.689A>G XP_011538796.1:p.Lys230Arg
XM_011540495.2:c.500A>G XP_011538797.1:p.Lys167Arg
XM_017000038.1:c.701A>G XP_016855527.1:p.Lys234Arg
XM_017000039.1:c.689A>G XP_016855528.1:p.Lys230Arg
XM_017000040.1:c.587A>G XP_016855529.1:p.Lys196Arg
XM_017000041.2:c.419A>G XP_016855530.1:p.Lys140Arg
XM_017000042.1:c.*93A>G XP_016855531.1:n.*93A>G
XM_024449826.1:c.689A>G XP_024305594.1:p.Lys230Arg
XM_024449860.1:c.476A>G XP_024305628.1:p.Lys159Arg
XM_024449871.1:c.476A>G XP_024305639.1:p.Lys159Arg
NM_001378226.1:c.689A>G NP_001365155.1:p.Lys230Arg
NM_001378227.1:c.689A>G NP_001365156.1:p.Lys230Arg
NM_001378228.1:c.587A>G NP_001365157.1:p.Lys196Arg
NM_001378229.1:c.500A>G NP_001365158.1:p.Lys167Arg
NM_001378230.1:c.476A>G NP_001365159.1:p.Lys159Arg
NM_001378231.1:c.*93A>G NP_001365160.1:n.*93A>G
NM_015836.4:c.758A>G MANE Select NP_056651.1:p.Lys253Arg