Canonical Allele Identifier: CA343767725

Gene: DARS2

Linked Data

• dbSNP Id: rs1653902186
• MyVariant Identifiers: chr1:g.173826740A>G (hg19) ; chr1:g.173857602A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857602A>G , CM000663.2:g.173857602A>G	GRCh38
NC_000001.10:g.173826740A>G , CM000663.1:g.173826740A>G	GRCh37
NC_000001.9:g.172093363A>G	NCBI36
NG_016138.1:g.37944A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1414A>G	ENSP00000497663.1:n.*1414A>G
ENST00000647645.1:c.1772A>G	ENSP00000497450.1:p.Asp591Gly
ENST00000647730.1:c.*1525A>G	ENSP00000497781.1:n.*1525A>G
ENST00000647788.1:c.*979A>G	ENSP00000497769.1:n.*979A>G
ENST00000648271.1:c.*2301A>G	ENSP00000497795.1:n.*2301A>G
ENST00000648807.1:c.1682A>G	ENSP00000497472.1:p.Asp561Gly
ENST00000648960.1:c.1352A>G	ENSP00000497091.1:p.Asp451Gly
ENST00000649067.1:c.*838A>G	ENSP00000497052.1:n.*838A>G
ENST00000649689.2:c.1835A>G MANE Select	ENSP00000497569.1:p.Asp612Gly
ENST00000361951.4:c.1835A>G	ENSP00000355086.4:p.Asp612Gly
ENST00000471476.1:n.657A>G
NM_018122.4:c.1835A>G	NP_060592.2:p.Asp612Gly
XM_006711427.2:c.1682A>G	XP_006711490.1:p.Asp561Gly
NM_001365212.1:c.1682A>G	NP_001352141.1:p.Asp561Gly
NM_018122.5:c.1835A>G MANE Select	NP_060592.2:p.Asp612Gly