Canonical Allele Identifier: CA421811934

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826708C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857570C>G , CM000663.2:g.173857570C>G	GRCh38
NC_000001.10:g.173826708C>G , CM000663.1:g.173826708C>G	GRCh37
NC_000001.9:g.172093331C>G	NCBI36
NG_016138.1:g.37912C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1382C>G	ENSP00000497663.1:n.*1382C>G
ENST00000647645.1:c.1740C>G	ENSP00000497450.1:p.Val580=
ENST00000647730.1:c.*1493C>G	ENSP00000497781.1:n.*1493C>G
ENST00000647788.1:c.*947C>G	ENSP00000497769.1:n.*947C>G
ENST00000648271.1:c.*2269C>G	ENSP00000497795.1:n.*2269C>G
ENST00000648807.1:c.1650C>G	ENSP00000497472.1:p.Val550=
ENST00000648960.1:c.1320C>G	ENSP00000497091.1:p.Val440=
ENST00000649067.1:c.*806C>G	ENSP00000497052.1:n.*806C>G
ENST00000649689.2:c.1803C>G MANE Select	ENSP00000497569.1:p.Val601=
ENST00000361951.4:c.1803C>G	ENSP00000355086.4:p.Val601=
ENST00000471476.1:n.625C>G
NM_018122.4:c.1803C>G	NP_060592.2:p.Val601=
XM_006711427.2:c.1650C>G	XP_006711490.1:p.Val550=
NM_001365212.1:c.1650C>G	NP_001352141.1:p.Val550=
NM_018122.5:c.1803C>G MANE Select	NP_060592.2:p.Val601=