Canonical Allele Identifier: CA1207913190

Gene: DARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857518G= , CM000663.2:g.173857518G=	GRCh38
NC_000001.10:g.173826656G= , CM000663.1:g.173826656G=	GRCh37
NC_000001.9:g.172093279G=	NCBI36
NG_016138.1:g.37860G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000471476.2:c.*1330G=	ENSP00000497663.1:n.*1330G=
ENST00000647645.1:c.1688G=	ENSP00000497450.1:p.Gly563=
ENST00000647730.1:c.*1441G=	ENSP00000497781.1:n.*1441G=
ENST00000647788.1:c.*895G=	ENSP00000497769.1:n.*895G=
ENST00000648271.1:c.*2217G=	ENSP00000497795.1:n.*2217G=
ENST00000648807.1:c.1598G=	ENSP00000497472.1:p.Gly533=
ENST00000648960.1:c.1268G=	ENSP00000497091.1:p.Gly423=
ENST00000649067.1:c.*754G=	ENSP00000497052.1:n.*754G=
ENST00000649689.2:c.1751G= MANE Select	ENSP00000497569.1:p.Gly584=
ENST00000361951.4:c.1751G=	ENSP00000355086.4:p.Gly584=
ENST00000471476.1:n.573G=
NM_018122.4:c.1751G=	NP_060592.2:p.Gly584=
XM_006711427.2:c.1598G=	XP_006711490.1:p.Gly533=
NM_001365212.1:c.1598G=	NP_001352141.1:p.Gly533=
NM_018122.5:c.1751G= MANE Select	NP_060592.2:p.Gly584=