Canonical Allele Identifier: CA891312935

Gene: DARS2

Linked Data

• dbSNP Id: rs1438437041
• gnomAD v4: 1-173838128-G-T
• MyVariant Identifiers: chr1:g.173807266G>T (hg19) ; chr1:g.173838128G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173838128G>T , CM000663.2:g.173838128G>T	GRCh38
NC_000001.10:g.173807266G>T , CM000663.1:g.173807266G>T	GRCh37
NC_000001.9:g.172073889G>T	NCBI36
NG_016138.1:g.18470G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000471476.2:c.*461-62G>T	ENSP00000497663.1:n.*461-62G>T
ENST00000647645.1:c.771-62G>T	ENSP00000497450.1:n.771-62G>T
ENST00000647730.1:c.*461-62G>T	ENSP00000497781.1:n.*461-62G>T
ENST00000647788.1:c.*461-62G>T	ENSP00000497769.1:n.*461-62G>T
ENST00000648271.1:c.*461-62G>T	ENSP00000497795.1:n.*461-62G>T
ENST00000648458.1:c.771-62G>T	ENSP00000497874.1:n.771-62G>T
ENST00000648807.1:c.771-62G>T	ENSP00000497472.1:n.771-62G>T
ENST00000648960.1:c.771-62G>T	ENSP00000497091.1:n.771-62G>T
ENST00000649067.1:c.771-62G>T	ENSP00000497052.1:n.771-62G>T
ENST00000649106.1:c.120-1239G>T
ENST00000649689.2:c.771-62G>T MANE Select	ENSP00000497569.1:n.771-62G>T
ENST00000650297.1:n.1154-62G>T
ENST00000361951.4:c.771-62G>T	ENSP00000355086.4:n.771-62G>T
NM_018122.4:c.771-62G>T	NP_060592.2:n.771-62G>T
XM_006711427.2:c.771-62G>T	XP_006711490.1:n.771-62G>T
XM_011509711.1:c.771-62G>T	XP_011508013.1:n.771-62G>T
NM_001365212.1:c.771-62G>T	NP_001352141.1:n.771-62G>T
NM_001365213.1:c.771-62G>T	NP_001352142.1:n.771-62G>T
NM_018122.5:c.771-62G>T MANE Select	NP_060592.2:n.771-62G>T
NM_001365213.2:c.771-62G>T	NP_001352142.1:n.771-62G>T