Canonical Allele Identifier: CA1207913239

Gene: DARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857689C= , CM000663.2:g.173857689C=	GRCh38
NC_000001.10:g.173826827C= , CM000663.1:g.173826827C=	GRCh37
NC_000001.9:g.172093450C=	NCBI36
NG_016138.1:g.38031C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1501C=	ENSP00000497663.1:n.*1501C=
ENST00000647645.1:c.1859C=	ENSP00000497450.1:p.Ala620=
ENST00000647730.1:c.*1612C=	ENSP00000497781.1:n.*1612C=
ENST00000647788.1:c.*1066C=	ENSP00000497769.1:n.*1066C=
ENST00000648271.1:c.*2388C=	ENSP00000497795.1:n.*2388C=
ENST00000648807.1:c.1769C=	ENSP00000497472.1:p.Ala590=
ENST00000648960.1:c.1439C=	ENSP00000497091.1:p.Ala480=
ENST00000649067.1:c.*925C=	ENSP00000497052.1:n.*925C=
ENST00000649689.2:c.1922C= MANE Select	ENSP00000497569.1:p.Ala641=
ENST00000361951.4:c.1922C=	ENSP00000355086.4:p.Ala641=
ENST00000471476.1:n.744C=
NM_018122.4:c.1922C=	NP_060592.2:p.Ala641=
XM_006711427.2:c.1769C=	XP_006711490.1:p.Ala590=
NM_001365212.1:c.1769C=	NP_001352141.1:p.Ala590=
NM_018122.5:c.1922C= MANE Select	NP_060592.2:p.Ala641=