Canonical Allele Identifier: CA421812047

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826801A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857663A>T , CM000663.2:g.173857663A>T	GRCh38
NC_000001.10:g.173826801A>T , CM000663.1:g.173826801A>T	GRCh37
NC_000001.9:g.172093424A>T	NCBI36
NG_016138.1:g.38005A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1475A>T	ENSP00000497663.1:n.*1475A>T
ENST00000647645.1:c.1833A>T	ENSP00000497450.1:p.Arg611=
ENST00000647730.1:c.*1586A>T	ENSP00000497781.1:n.*1586A>T
ENST00000647788.1:c.*1040A>T	ENSP00000497769.1:n.*1040A>T
ENST00000648271.1:c.*2362A>T	ENSP00000497795.1:n.*2362A>T
ENST00000648807.1:c.1743A>T	ENSP00000497472.1:p.Arg581=
ENST00000648960.1:c.1413A>T	ENSP00000497091.1:p.Arg471=
ENST00000649067.1:c.*899A>T	ENSP00000497052.1:n.*899A>T
ENST00000649689.2:c.1896A>T MANE Select	ENSP00000497569.1:p.Arg632=
ENST00000361951.4:c.1896A>T	ENSP00000355086.4:p.Arg632=
ENST00000471476.1:n.718A>T
NM_018122.4:c.1896A>T	NP_060592.2:p.Arg632=
XM_006711427.2:c.1743A>T	XP_006711490.1:p.Arg581=
NM_001365212.1:c.1743A>T	NP_001352141.1:p.Arg581=
NM_018122.5:c.1896A>T MANE Select	NP_060592.2:p.Arg632=