Canonical Allele Identifier: CA514276964
Community Standard Title: NM_000343.4(SLC5A1):c.1191C>T (p.Ile397=)
Gene: SLC5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32091673C>T , CM000684.2:g.32091673C>T GRCh38
NC_000022.10:g.32487660C>T , CM000684.1:g.32487660C>T GRCh37
NC_000022.9:g.30817660C>T NCBI36
NG_017045.1:g.53642C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000343.4:c.1191C>T MANE Select NP_000334.1:p.Ile397=
ENST00000266088.9:c.1191C>T MANE Select ENSP00000266088.4:p.Ile397=
NM_000343.3:c.1191C>T NP_000334.1:p.Ile397=
NM_001256314.1:c.810C>T NP_001243243.1:p.Ile270=
NM_001256314.2:c.810C>T NP_001243243.1:p.Ile270=
ENST00000266088.8:c.1191C>T ENSP00000266088.4:p.Ile397=
ENST00000477969.1:n.357C>T
ENST00000543737.2:c.810C>T ENSP00000444898.1:p.Ile270=
XM_011530331.1:c.1191C>T XP_011528633.1:p.Ile397=
XR_938173.1:n.591+15165G>A
XR_938174.1:n.487-22870G>A