Canonical Allele Identifier: CA343767549

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826655G>A (hg19) ; chr1:g.173857517G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857517G>A , CM000663.2:g.173857517G>A	GRCh38
NC_000001.10:g.173826655G>A , CM000663.1:g.173826655G>A	GRCh37
NC_000001.9:g.172093278G>A	NCBI36
NG_016138.1:g.37859G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1330-1G>A	ENSP00000497663.1:n.*1330-1G>A
ENST00000647645.1:c.1688-1G>A	ENSP00000497450.1:n.1688-1G>A
ENST00000647730.1:c.*1441-1G>A	ENSP00000497781.1:n.*1441-1G>A
ENST00000647788.1:c.*895-1G>A	ENSP00000497769.1:n.*895-1G>A
ENST00000648271.1:c.*2216G>A	ENSP00000497795.1:n.*2216G>A
ENST00000648807.1:c.1598-1G>A	ENSP00000497472.1:n.1598-1G>A
ENST00000648960.1:c.1268-1G>A	ENSP00000497091.1:n.1268-1G>A
ENST00000649067.1:c.*753G>A	ENSP00000497052.1:n.*753G>A
ENST00000649689.2:c.1751-1G>A MANE Select	ENSP00000497569.1:n.1751-1G>A
ENST00000361951.4:c.1751-1G>A	ENSP00000355086.4:n.1751-1G>A
ENST00000471476.1:n.573-1G>A
NM_018122.4:c.1751-1G>A	NP_060592.2:n.1751-1G>A
XM_006711427.2:c.1598-1G>A	XP_006711490.1:n.1598-1G>A
NM_001365212.1:c.1598-1G>A	NP_001352141.1:n.1598-1G>A
NM_018122.5:c.1751-1G>A MANE Select	NP_060592.2:n.1751-1G>A