Canonical Allele Identifier: CA3075481
Community Standard Title: NM_031291.4(SLC25A31):c.206G>A (p.Cys69Tyr)
Gene: SLC25A31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127730751G>A , CM000666.2:g.127730751G>A GRCh38
NC_000004.11:g.128651906G>A , CM000666.1:g.128651906G>A GRCh37
NC_000004.10:g.128871356G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_031291.4:c.206G>A MANE Select NP_112581.1:p.Cys69Tyr
ENST00000281154.6:c.206G>A MANE Select ENSP00000281154.4:p.Cys69Tyr
NM_001318467.1:c.206G>A NP_001305396.1:p.Cys69Tyr
NM_001318467.2:c.206G>A NP_001305396.1:p.Cys69Tyr
NM_031291.2:c.206G>A NP_112581.1:p.Cys69Tyr
NM_031291.3:c.206G>A NP_112581.1:p.Cys69Tyr
ENST00000281154.5:c.206G>A ENSP00000281154.4:p.Cys69Tyr
XM_011532297.1:c.206G>A XP_011530599.1:p.Cys69Tyr
XM_011532298.1:c.206G>A XP_011530600.1:p.Cys69Tyr
XM_011532298.2:c.206G>A XP_011530600.1:p.Cys69Tyr