Canonical Allele Identifier: CA1207913215

Gene: DARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857599A= , CM000663.2:g.173857599A=	GRCh38
NC_000001.10:g.173826737A= , CM000663.1:g.173826737A=	GRCh37
NC_000001.9:g.172093360A=	NCBI36
NG_016138.1:g.37941A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000471476.2:c.*1411A=	ENSP00000497663.1:n.*1411A=
ENST00000647645.1:c.1769A=	ENSP00000497450.1:p.His590=
ENST00000647730.1:c.*1522A=	ENSP00000497781.1:n.*1522A=
ENST00000647788.1:c.*976A=	ENSP00000497769.1:n.*976A=
ENST00000648271.1:c.*2298A=	ENSP00000497795.1:n.*2298A=
ENST00000648807.1:c.1679A=	ENSP00000497472.1:p.His560=
ENST00000648960.1:c.1349A=	ENSP00000497091.1:p.His450=
ENST00000649067.1:c.*835A=	ENSP00000497052.1:n.*835A=
ENST00000649689.2:c.1832A= MANE Select	ENSP00000497569.1:p.His611=
ENST00000361951.4:c.1832A=	ENSP00000355086.4:p.His611=
ENST00000471476.1:n.654A=
NM_018122.4:c.1832A=	NP_060592.2:p.His611=
XM_006711427.2:c.1679A=	XP_006711490.1:p.His560=
NM_001365212.1:c.1679A=	NP_001352141.1:p.His560=
NM_018122.5:c.1832A= MANE Select	NP_060592.2:p.His611=