Canonical Allele Identifier: CA343767737

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826746T>A (hg19) ; chr1:g.173857608T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857608T>A , CM000663.2:g.173857608T>A	GRCh38
NC_000001.10:g.173826746T>A , CM000663.1:g.173826746T>A	GRCh37
NC_000001.9:g.172093369T>A	NCBI36
NG_016138.1:g.37950T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1420T>A	ENSP00000497663.1:n.*1420T>A
ENST00000647645.1:c.1778T>A	ENSP00000497450.1:p.Met593Lys
ENST00000647730.1:c.*1531T>A	ENSP00000497781.1:n.*1531T>A
ENST00000647788.1:c.*985T>A	ENSP00000497769.1:n.*985T>A
ENST00000648271.1:c.*2307T>A	ENSP00000497795.1:n.*2307T>A
ENST00000648807.1:c.1688T>A	ENSP00000497472.1:p.Met563Lys
ENST00000648960.1:c.1358T>A	ENSP00000497091.1:p.Met453Lys
ENST00000649067.1:c.*844T>A	ENSP00000497052.1:n.*844T>A
ENST00000649689.2:c.1841T>A MANE Select	ENSP00000497569.1:p.Met614Lys
ENST00000361951.4:c.1841T>A	ENSP00000355086.4:p.Met614Lys
ENST00000471476.1:n.663T>A
NM_018122.4:c.1841T>A	NP_060592.2:p.Met614Lys
XM_006711427.2:c.1688T>A	XP_006711490.1:p.Met563Lys
NM_001365212.1:c.1688T>A	NP_001352141.1:p.Met563Lys
NM_018122.5:c.1841T>A MANE Select	NP_060592.2:p.Met614Lys