Canonical Allele Identifier: CA1207913214
Gene: DARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857596G= , CM000663.2:g.173857596G= GRCh38
NC_000001.10:g.173826734G= , CM000663.1:g.173826734G= GRCh37
NC_000001.9:g.172093357G= NCBI36
NG_016138.1:g.37938G=

Transcript Alleles

HGVS Amino-acid change
ENST00000471476.2:c.*1408G= ENSP00000497663.1:n.*1408G=
ENST00000647645.1:c.1766G= ENSP00000497450.1:p.Gly589=
ENST00000647730.1:c.*1519G= ENSP00000497781.1:n.*1519G=
ENST00000647788.1:c.*973G= ENSP00000497769.1:n.*973G=
ENST00000648271.1:c.*2295G= ENSP00000497795.1:n.*2295G=
ENST00000648807.1:c.1676G= ENSP00000497472.1:p.Gly559=
ENST00000648960.1:c.1346G= ENSP00000497091.1:p.Gly449=
ENST00000649067.1:c.*832G= ENSP00000497052.1:n.*832G=
ENST00000649689.2:c.1829G= MANE Select ENSP00000497569.1:p.Gly610=
ENST00000361951.4:c.1829G= ENSP00000355086.4:p.Gly610=
ENST00000471476.1:n.651G=
NM_018122.4:c.1829G= NP_060592.2:p.Gly610=
XM_006711427.2:c.1676G= XP_006711490.1:p.Gly559=
NM_001365212.1:c.1676G= NP_001352141.1:p.Gly559=
NM_018122.5:c.1829G= MANE Select NP_060592.2:p.Gly610=