Canonical Allele Identifier: CA10198074
Community Standard Title: NM_000343.4(SLC5A1):c.875G>A (p.Cys292Tyr)
Gene: SLC5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32084649G>A , CM000684.2:g.32084649G>A GRCh38
NC_000022.10:g.32480636G>A , CM000684.1:g.32480636G>A GRCh37
NC_000022.9:g.30810636G>A NCBI36
NG_017045.1:g.46618G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000343.4:c.875G>A MANE Select NP_000334.1:p.Cys292Tyr
ENST00000266088.9:c.875G>A MANE Select ENSP00000266088.4:p.Cys292Tyr
NM_000343.3:c.875G>A NP_000334.1:p.Cys292Tyr
NM_001256314.1:c.494G>A NP_001243243.1:p.Cys165Tyr
NM_001256314.2:c.494G>A NP_001243243.1:p.Cys165Tyr
ENST00000266088.8:c.875G>A ENSP00000266088.4:p.Cys292Tyr
ENST00000486394.1:n.315G>A
ENST00000543737.2:c.494G>A ENSP00000444898.1:p.Cys165Tyr
XM_011530331.1:c.875G>A XP_011528633.1:p.Cys292Tyr
XR_938173.1:n.592-15846C>T
XR_938174.1:n.487-15846C>T