Canonical Allele Identifier: CA1207913178

Gene: DARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857488T= , CM000663.2:g.173857488T=	GRCh38
NC_000001.10:g.173826626T= , CM000663.1:g.173826626T=	GRCh37
NC_000001.9:g.172093249T=	NCBI36
NG_016138.1:g.37830T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1330-30T=	ENSP00000497663.1:n.*1330-30T=
ENST00000647645.1:c.1688-30T=	ENSP00000497450.1:n.1688-30T=
ENST00000647730.1:c.*1441-30T=	ENSP00000497781.1:n.*1441-30T=
ENST00000647788.1:c.*895-30T=	ENSP00000497769.1:n.*895-30T=
ENST00000648271.1:c.*2187T=	ENSP00000497795.1:n.*2187T=
ENST00000648807.1:c.1598-30T=	ENSP00000497472.1:n.1598-30T=
ENST00000648960.1:c.1268-30T=	ENSP00000497091.1:n.1268-30T=
ENST00000649067.1:c.*724T=	ENSP00000497052.1:n.*724T=
ENST00000649689.2:c.1751-30T= MANE Select	ENSP00000497569.1:n.1751-30T=
ENST00000361951.4:c.1751-30T=	ENSP00000355086.4:n.1751-30T=
ENST00000471476.1:n.573-30T=
NM_018122.4:c.1751-30T=	NP_060592.2:n.1751-30T=
XM_006711427.2:c.1598-30T=	XP_006711490.1:n.1598-30T=
NM_001365212.1:c.1598-30T=	NP_001352141.1:n.1598-30T=
NM_018122.5:c.1751-30T= MANE Select	NP_060592.2:n.1751-30T=