Canonical Allele Identifier: CA2573953301

Gene: DARS2

Linked Data

• gnomAD v4: 1-173838138-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173838138G>A , CM000663.2:g.173838138G>A	GRCh38
NC_000001.10:g.173807276G>A , CM000663.1:g.173807276G>A	GRCh37
NC_000001.9:g.172073899G>A	NCBI36
NG_016138.1:g.18480G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000471476.2:c.*461-52G>A	ENSP00000497663.1:n.*461-52G>A
ENST00000647645.1:c.771-52G>A	ENSP00000497450.1:n.771-52G>A
ENST00000647730.1:c.*461-52G>A	ENSP00000497781.1:n.*461-52G>A
ENST00000647788.1:c.*461-52G>A	ENSP00000497769.1:n.*461-52G>A
ENST00000648271.1:c.*461-52G>A	ENSP00000497795.1:n.*461-52G>A
ENST00000648458.1:c.771-52G>A	ENSP00000497874.1:n.771-52G>A
ENST00000648807.1:c.771-52G>A	ENSP00000497472.1:n.771-52G>A
ENST00000648960.1:c.771-52G>A	ENSP00000497091.1:n.771-52G>A
ENST00000649067.1:c.771-52G>A	ENSP00000497052.1:n.771-52G>A
ENST00000649106.1:c.120-1229G>A
ENST00000649689.2:c.771-52G>A MANE Select	ENSP00000497569.1:n.771-52G>A
ENST00000650297.1:n.1154-52G>A
ENST00000361951.4:c.771-52G>A	ENSP00000355086.4:n.771-52G>A
NM_018122.4:c.771-52G>A	NP_060592.2:n.771-52G>A
XM_006711427.2:c.771-52G>A	XP_006711490.1:n.771-52G>A
XM_011509711.1:c.771-52G>A	XP_011508013.1:n.771-52G>A
NM_001365212.1:c.771-52G>A	NP_001352141.1:n.771-52G>A
NM_001365213.1:c.771-52G>A	NP_001352142.1:n.771-52G>A
NM_018122.5:c.771-52G>A MANE Select	NP_060592.2:n.771-52G>A
NM_001365213.2:c.771-52G>A	NP_001352142.1:n.771-52G>A