Canonical Allele Identifier: CA1207913212

Gene: DARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857582A= , CM000663.2:g.173857582A=	GRCh38
NC_000001.10:g.173826720A= , CM000663.1:g.173826720A=	GRCh37
NC_000001.9:g.172093343A=	NCBI36
NG_016138.1:g.37924A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1394A=	ENSP00000497663.1:n.*1394A=
ENST00000647645.1:c.1752A=	ENSP00000497450.1:p.Pro584=
ENST00000647730.1:c.*1505A=	ENSP00000497781.1:n.*1505A=
ENST00000647788.1:c.*959A=	ENSP00000497769.1:n.*959A=
ENST00000648271.1:c.*2281A=	ENSP00000497795.1:n.*2281A=
ENST00000648807.1:c.1662A=	ENSP00000497472.1:p.Pro554=
ENST00000648960.1:c.1332A=	ENSP00000497091.1:p.Pro444=
ENST00000649067.1:c.*818A=	ENSP00000497052.1:n.*818A=
ENST00000649689.2:c.1815A= MANE Select	ENSP00000497569.1:p.Pro605=
ENST00000361951.4:c.1815A=	ENSP00000355086.4:p.Pro605=
ENST00000471476.1:n.637A=
NM_018122.4:c.1815A=	NP_060592.2:p.Pro605=
XM_006711427.2:c.1662A=	XP_006711490.1:p.Pro554=
NM_001365212.1:c.1662A=	NP_001352141.1:p.Pro554=
NM_018122.5:c.1815A= MANE Select	NP_060592.2:p.Pro605=