Canonical Allele Identifier: CA1207913192

Gene: DARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857522A= , CM000663.2:g.173857522A=	GRCh38
NC_000001.10:g.173826660A= , CM000663.1:g.173826660A=	GRCh37
NC_000001.9:g.172093283A=	NCBI36
NG_016138.1:g.37864A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000471476.2:c.*1334A=	ENSP00000497663.1:n.*1334A=
ENST00000647645.1:c.1692A=	ENSP00000497450.1:p.Leu564=
ENST00000647730.1:c.*1445A=	ENSP00000497781.1:n.*1445A=
ENST00000647788.1:c.*899A=	ENSP00000497769.1:n.*899A=
ENST00000648271.1:c.*2221A=	ENSP00000497795.1:n.*2221A=
ENST00000648807.1:c.1602A=	ENSP00000497472.1:p.Leu534=
ENST00000648960.1:c.1272A=	ENSP00000497091.1:p.Leu424=
ENST00000649067.1:c.*758A=	ENSP00000497052.1:n.*758A=
ENST00000649689.2:c.1755A= MANE Select	ENSP00000497569.1:p.Leu585=
ENST00000361951.4:c.1755A=	ENSP00000355086.4:p.Leu585=
ENST00000471476.1:n.577A=
NM_018122.4:c.1755A=	NP_060592.2:p.Leu585=
XM_006711427.2:c.1602A=	XP_006711490.1:p.Leu534=
NM_001365212.1:c.1602A=	NP_001352141.1:p.Leu534=
NM_018122.5:c.1755A= MANE Select	NP_060592.2:p.Leu585=