Canonical Allele Identifier: CA10198066
Community Standard Title: NM_000343.4(SLC5A1):c.799C>T (p.Arg267Ter)
Gene: SLC5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32084573C>T , CM000684.2:g.32084573C>T GRCh38
NC_000022.10:g.32480560C>T , CM000684.1:g.32480560C>T GRCh37
NC_000022.9:g.30810560C>T NCBI36
NG_017045.1:g.46542C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000343.4:c.799C>T MANE Select NP_000334.1:p.Arg267Ter
ENST00000266088.9:c.799C>T MANE Select ENSP00000266088.4:p.Arg267Ter
NM_000343.3:c.799C>T NP_000334.1:p.Arg267Ter
NM_001256314.1:c.418C>T NP_001243243.1:p.Arg140Ter
NM_001256314.2:c.418C>T NP_001243243.1:p.Arg140Ter
ENST00000266088.8:c.799C>T ENSP00000266088.4:p.Arg267Ter
ENST00000486394.1:n.239C>T
ENST00000543737.2:c.418C>T ENSP00000444898.1:p.Arg140Ter
XM_011530331.1:c.799C>T XP_011528633.1:p.Arg267Ter
XR_938173.1:n.592-15770G>A
XR_938174.1:n.487-15770G>A