Canonical Allele Identifier: CA1207913193

Gene: DARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857523G= , CM000663.2:g.173857523G=	GRCh38
NC_000001.10:g.173826661G= , CM000663.1:g.173826661G=	GRCh37
NC_000001.9:g.172093284G=	NCBI36
NG_016138.1:g.37865G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1335G=	ENSP00000497663.1:n.*1335G=
ENST00000647645.1:c.1693G=	ENSP00000497450.1:p.Asp565=
ENST00000647730.1:c.*1446G=	ENSP00000497781.1:n.*1446G=
ENST00000647788.1:c.*900G=	ENSP00000497769.1:n.*900G=
ENST00000648271.1:c.*2222G=	ENSP00000497795.1:n.*2222G=
ENST00000648807.1:c.1603G=	ENSP00000497472.1:p.Asp535=
ENST00000648960.1:c.1273G=	ENSP00000497091.1:p.Asp425=
ENST00000649067.1:c.*759G=	ENSP00000497052.1:n.*759G=
ENST00000649689.2:c.1756G= MANE Select	ENSP00000497569.1:p.Asp586=
ENST00000361951.4:c.1756G=	ENSP00000355086.4:p.Asp586=
ENST00000471476.1:n.578G=
NM_018122.4:c.1756G=	NP_060592.2:p.Asp586=
XM_006711427.2:c.1603G=	XP_006711490.1:p.Asp535=
NM_001365212.1:c.1603G=	NP_001352141.1:p.Asp535=
NM_018122.5:c.1756G= MANE Select	NP_060592.2:p.Asp586=