Canonical Allele Identifier: CA343762242

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173807332T>G (hg19) ; chr1:g.173838194T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173838194T>G , CM000663.2:g.173838194T>G	GRCh38
NC_000001.10:g.173807332T>G , CM000663.1:g.173807332T>G	GRCh37
NC_000001.9:g.172073955T>G	NCBI36
NG_016138.1:g.18536T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*465T>G	ENSP00000497663.1:n.*465T>G
ENST00000647645.1:c.775T>G	ENSP00000497450.1:p.Phe259Val
ENST00000647730.1:c.*465T>G	ENSP00000497781.1:n.*465T>G
ENST00000647788.1:c.*465T>G	ENSP00000497769.1:n.*465T>G
ENST00000648271.1:c.*465T>G	ENSP00000497795.1:n.*465T>G
ENST00000648458.1:c.775T>G	ENSP00000497874.1:p.Phe259Val
ENST00000648807.1:c.775T>G	ENSP00000497472.1:p.Phe259Val
ENST00000648960.1:c.775T>G	ENSP00000497091.1:p.Phe259Val
ENST00000649067.1:c.775T>G	ENSP00000497052.1:p.Phe259Val
ENST00000649106.1:c.120-1173T>G
ENST00000649689.2:c.775T>G MANE Select	ENSP00000497569.1:p.Phe259Val
ENST00000650297.1:n.1158T>G
ENST00000361951.4:c.775T>G	ENSP00000355086.4:p.Phe259Val
NM_018122.4:c.775T>G	NP_060592.2:p.Phe259Val
XM_006711427.2:c.775T>G	XP_006711490.1:p.Phe259Val
XM_011509711.1:c.775T>G	XP_011508013.1:p.Phe259Val
NM_001365212.1:c.775T>G	NP_001352141.1:p.Phe259Val
NM_001365213.1:c.775T>G	NP_001352142.1:p.Phe259Val
NM_018122.5:c.775T>G MANE Select	NP_060592.2:p.Phe259Val
NM_001365213.2:c.775T>G	NP_001352142.1:p.Phe259Val