Canonical Allele Identifier: CA343767631

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826696C>A (hg19) ; chr1:g.173857558C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857558C>A , CM000663.2:g.173857558C>A	GRCh38
NC_000001.10:g.173826696C>A , CM000663.1:g.173826696C>A	GRCh37
NC_000001.9:g.172093319C>A	NCBI36
NG_016138.1:g.37900C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1370C>A	ENSP00000497663.1:n.*1370C>A
ENST00000647645.1:c.1728C>A	ENSP00000497450.1:p.Ser576Arg
ENST00000647730.1:c.*1481C>A	ENSP00000497781.1:n.*1481C>A
ENST00000647788.1:c.*935C>A	ENSP00000497769.1:n.*935C>A
ENST00000648271.1:c.*2257C>A	ENSP00000497795.1:n.*2257C>A
ENST00000648807.1:c.1638C>A	ENSP00000497472.1:p.Ser546Arg
ENST00000648960.1:c.1308C>A	ENSP00000497091.1:p.Ser436Arg
ENST00000649067.1:c.*794C>A	ENSP00000497052.1:n.*794C>A
ENST00000649689.2:c.1791C>A MANE Select	ENSP00000497569.1:p.Ser597Arg
ENST00000361951.4:c.1791C>A	ENSP00000355086.4:p.Ser597Arg
ENST00000471476.1:n.613C>A
NM_018122.4:c.1791C>A	NP_060592.2:p.Ser597Arg
XM_006711427.2:c.1638C>A	XP_006711490.1:p.Ser546Arg
NM_001365212.1:c.1638C>A	NP_001352141.1:p.Ser546Arg
NM_018122.5:c.1791C>A MANE Select	NP_060592.2:p.Ser597Arg