Canonical Allele Identifier: CA421811945

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826714C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857576C>G , CM000663.2:g.173857576C>G	GRCh38
NC_000001.10:g.173826714C>G , CM000663.1:g.173826714C>G	GRCh37
NC_000001.9:g.172093337C>G	NCBI36
NG_016138.1:g.37918C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1388C>G	ENSP00000497663.1:n.*1388C>G
ENST00000647645.1:c.1746C>G	ENSP00000497450.1:p.Ala582=
ENST00000647730.1:c.*1499C>G	ENSP00000497781.1:n.*1499C>G
ENST00000647788.1:c.*953C>G	ENSP00000497769.1:n.*953C>G
ENST00000648271.1:c.*2275C>G	ENSP00000497795.1:n.*2275C>G
ENST00000648807.1:c.1656C>G	ENSP00000497472.1:p.Ala552=
ENST00000648960.1:c.1326C>G	ENSP00000497091.1:p.Ala442=
ENST00000649067.1:c.*812C>G	ENSP00000497052.1:n.*812C>G
ENST00000649689.2:c.1809C>G MANE Select	ENSP00000497569.1:p.Ala603=
ENST00000361951.4:c.1809C>G	ENSP00000355086.4:p.Ala603=
ENST00000471476.1:n.631C>G
NM_018122.4:c.1809C>G	NP_060592.2:p.Ala603=
XM_006711427.2:c.1656C>G	XP_006711490.1:p.Ala552=
NM_001365212.1:c.1656C>G	NP_001352141.1:p.Ala552=
NM_018122.5:c.1809C>G MANE Select	NP_060592.2:p.Ala603=