Canonical Allele Identifier: CA421812067

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826816A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857678A>G , CM000663.2:g.173857678A>G	GRCh38
NC_000001.10:g.173826816A>G , CM000663.1:g.173826816A>G	GRCh37
NC_000001.9:g.172093439A>G	NCBI36
NG_016138.1:g.38020A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1490A>G	ENSP00000497663.1:n.*1490A>G
ENST00000647645.1:c.1848A>G	ENSP00000497450.1:p.Thr616=
ENST00000647730.1:c.*1601A>G	ENSP00000497781.1:n.*1601A>G
ENST00000647788.1:c.*1055A>G	ENSP00000497769.1:n.*1055A>G
ENST00000648271.1:c.*2377A>G	ENSP00000497795.1:n.*2377A>G
ENST00000648807.1:c.1758A>G	ENSP00000497472.1:p.Thr586=
ENST00000648960.1:c.1428A>G	ENSP00000497091.1:p.Thr476=
ENST00000649067.1:c.*914A>G	ENSP00000497052.1:n.*914A>G
ENST00000649689.2:c.1911A>G MANE Select	ENSP00000497569.1:p.Thr637=
ENST00000361951.4:c.1911A>G	ENSP00000355086.4:p.Thr637=
ENST00000471476.1:n.733A>G
NM_018122.4:c.1911A>G	NP_060592.2:p.Thr637=
XM_006711427.2:c.1758A>G	XP_006711490.1:p.Thr586=
NM_001365212.1:c.1758A>G	NP_001352141.1:p.Thr586=
NM_018122.5:c.1911A>G MANE Select	NP_060592.2:p.Thr637=