Canonical Allele Identifier: CA1207903348
Gene: DARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173833389T= , CM000663.2:g.173833389T= GRCh38
NC_000001.10:g.173802527T= , CM000663.1:g.173802527T= GRCh37
NC_000001.9:g.172069150T= NCBI36
NG_016138.1:g.13731T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*196T= ENSP00000497663.1:n.*196T=
ENST00000647645.1:c.506T= ENSP00000497450.1:p.Leu169=
ENST00000647730.1:c.*196T= ENSP00000497781.1:n.*196T=
ENST00000647788.1:c.*196T= ENSP00000497769.1:n.*196T=
ENST00000648271.1:c.*196T= ENSP00000497795.1:n.*196T=
ENST00000648458.1:c.506T= ENSP00000497874.1:p.Leu169=
ENST00000648807.1:c.506T= ENSP00000497472.1:p.Leu169=
ENST00000648960.1:c.506T= ENSP00000497091.1:p.Leu169=
ENST00000649067.1:c.506T= ENSP00000497052.1:p.Leu169=
ENST00000649689.2:c.506T= MANE Select ENSP00000497569.1:p.Leu169=
ENST00000650297.1:n.889T=
ENST00000361951.4:c.506T= ENSP00000355086.4:p.Leu169=
NM_018122.4:c.506T= NP_060592.2:p.Leu169=
XM_006711427.2:c.506T= XP_006711490.1:p.Leu169=
XM_011509711.1:c.506T= XP_011508013.1:p.Leu169=
NM_001365212.1:c.506T= NP_001352141.1:p.Leu169=
NM_001365213.1:c.506T= NP_001352142.1:p.Leu169=
NM_018122.5:c.506T= MANE Select NP_060592.2:p.Leu169=
NM_001365213.2:c.506T= NP_001352142.1:p.Leu169=