Canonical Allele Identifier: CA343767605
Gene: DARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857544A>T , CM000663.2:g.173857544A>T GRCh38
NC_000001.10:g.173826682A>T , CM000663.1:g.173826682A>T GRCh37
NC_000001.9:g.172093305A>T NCBI36
NG_016138.1:g.37886A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*1356A>T ENSP00000497663.1:n.*1356A>T
ENST00000647645.1:c.1714A>T ENSP00000497450.1:p.Thr572Ser
ENST00000647730.1:c.*1467A>T ENSP00000497781.1:n.*1467A>T
ENST00000647788.1:c.*921A>T ENSP00000497769.1:n.*921A>T
ENST00000648271.1:c.*2243A>T ENSP00000497795.1:n.*2243A>T
ENST00000648807.1:c.1624A>T ENSP00000497472.1:p.Thr542Ser
ENST00000648960.1:c.1294A>T ENSP00000497091.1:p.Thr432Ser
ENST00000649067.1:c.*780A>T ENSP00000497052.1:n.*780A>T
ENST00000649689.2:c.1777A>T MANE Select ENSP00000497569.1:p.Thr593Ser
ENST00000361951.4:c.1777A>T ENSP00000355086.4:p.Thr593Ser
ENST00000471476.1:n.599A>T
NM_018122.4:c.1777A>T NP_060592.2:p.Thr593Ser
XM_006711427.2:c.1624A>T XP_006711490.1:p.Thr542Ser
NM_001365212.1:c.1624A>T NP_001352141.1:p.Thr542Ser
NM_018122.5:c.1777A>T MANE Select NP_060592.2:p.Thr593Ser