Canonical Allele Identifier: CA421811971

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826735A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857597A>G , CM000663.2:g.173857597A>G	GRCh38
NC_000001.10:g.173826735A>G , CM000663.1:g.173826735A>G	GRCh37
NC_000001.9:g.172093358A>G	NCBI36
NG_016138.1:g.37939A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000471476.2:c.*1409A>G	ENSP00000497663.1:n.*1409A>G
ENST00000647645.1:c.1767A>G	ENSP00000497450.1:p.Gly589=
ENST00000647730.1:c.*1520A>G	ENSP00000497781.1:n.*1520A>G
ENST00000647788.1:c.*974A>G	ENSP00000497769.1:n.*974A>G
ENST00000648271.1:c.*2296A>G	ENSP00000497795.1:n.*2296A>G
ENST00000648807.1:c.1677A>G	ENSP00000497472.1:p.Gly559=
ENST00000648960.1:c.1347A>G	ENSP00000497091.1:p.Gly449=
ENST00000649067.1:c.*833A>G	ENSP00000497052.1:n.*833A>G
ENST00000649689.2:c.1830A>G MANE Select	ENSP00000497569.1:p.Gly610=
ENST00000361951.4:c.1830A>G	ENSP00000355086.4:p.Gly610=
ENST00000471476.1:n.652A>G
NM_018122.4:c.1830A>G	NP_060592.2:p.Gly610=
XM_006711427.2:c.1677A>G	XP_006711490.1:p.Gly559=
NM_001365212.1:c.1677A>G	NP_001352141.1:p.Gly559=
NM_018122.5:c.1830A>G MANE Select	NP_060592.2:p.Gly610=