Canonical Allele Identifier: CA343758680
Community Standard Title: NM_018122.5(DARS2):c.382G>A (p.Gly128Arg)
Gene: DARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173830747G>A , CM000663.2:g.173830747G>A GRCh38
NC_000001.10:g.173799885G>A , CM000663.1:g.173799885G>A GRCh37
NC_000001.9:g.172066508G>A NCBI36
NG_016138.1:g.11089G>A

Transcript Alleles

HGVS Amino-acid Change
NM_018122.5:c.382G>A MANE Select NP_060592.2:p.Gly128Arg
ENST00000649689.2:c.382G>A MANE Select ENSP00000497569.1:p.Gly128Arg
NM_001365212.1:c.382G>A NP_001352141.1:p.Gly128Arg
NM_001365213.1:c.382G>A NP_001352142.1:p.Gly128Arg
NM_001365213.2:c.382G>A NP_001352142.1:p.Gly128Arg
NM_018122.4:c.382G>A NP_060592.2:p.Gly128Arg
ENST00000361951.4:c.382G>A ENSP00000355086.4:p.Gly128Arg
ENST00000471476.2:c.*72G>A ENSP00000497663.1:n.*72G>A
ENST00000647645.1:c.382G>A ENSP00000497450.1:p.Gly128Arg
ENST00000647730.1:c.*72G>A ENSP00000497781.1:n.*72G>A
ENST00000647788.1:c.*72G>A ENSP00000497769.1:n.*72G>A
ENST00000648055.1:n.2315G>A
ENST00000648271.1:c.*72G>A ENSP00000497795.1:n.*72G>A
ENST00000648458.1:c.382G>A ENSP00000497874.1:p.Gly128Arg
ENST00000648807.1:c.382G>A ENSP00000497472.1:p.Gly128Arg
ENST00000648960.1:c.382G>A ENSP00000497091.1:p.Gly128Arg
ENST00000649067.1:c.382G>A ENSP00000497052.1:p.Gly128Arg
ENST00000650297.1:n.765G>A
XM_006711427.2:c.382G>A XP_006711490.1:p.Gly128Arg
XM_011509711.1:c.382G>A XP_011508013.1:p.Gly128Arg