Canonical Allele Identifier: CA1207913203

Gene: DARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857556A= , CM000663.2:g.173857556A=	GRCh38
NC_000001.10:g.173826694A= , CM000663.1:g.173826694A=	GRCh37
NC_000001.9:g.172093317A=	NCBI36
NG_016138.1:g.37898A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1368A=	ENSP00000497663.1:n.*1368A=
ENST00000647645.1:c.1726A=	ENSP00000497450.1:p.Ser576=
ENST00000647730.1:c.*1479A=	ENSP00000497781.1:n.*1479A=
ENST00000647788.1:c.*933A=	ENSP00000497769.1:n.*933A=
ENST00000648271.1:c.*2255A=	ENSP00000497795.1:n.*2255A=
ENST00000648807.1:c.1636A=	ENSP00000497472.1:p.Ser546=
ENST00000648960.1:c.1306A=	ENSP00000497091.1:p.Ser436=
ENST00000649067.1:c.*792A=	ENSP00000497052.1:n.*792A=
ENST00000649689.2:c.1789A= MANE Select	ENSP00000497569.1:p.Ser597=
ENST00000361951.4:c.1789A=	ENSP00000355086.4:p.Ser597=
ENST00000471476.1:n.611A=
NM_018122.4:c.1789A=	NP_060592.2:p.Ser597=
XM_006711427.2:c.1636A=	XP_006711490.1:p.Ser546=
NM_001365212.1:c.1636A=	NP_001352141.1:p.Ser546=
NM_018122.5:c.1789A= MANE Select	NP_060592.2:p.Ser597=