Canonical Allele Identifier: CA514277457
Gene: SLC5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32500856C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32104869C>T , CM000684.2:g.32104869C>T GRCh38
NC_000022.10:g.32500856C>T , CM000684.1:g.32500856C>T GRCh37
NC_000022.9:g.30830856C>T NCBI36
NG_017045.1:g.66838C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266088.9:c.1749C>T MANE Select ENSP00000266088.4:p.Gly583=
ENST00000266088.8:c.1749C>T ENSP00000266088.4:p.Gly583=
ENST00000543737.2:c.1368C>T ENSP00000444898.1:p.Gly456=
NM_000343.3:c.1749C>T NP_000334.1:p.Gly583=
NM_001256314.1:c.1368C>T NP_001243243.1:p.Gly456=
XR_938173.1:n.591+1969G>A
XR_938174.1:n.486+14986G>A
NM_000343.4:c.1749C>T MANE Select NP_000334.1:p.Gly583=
NM_001256314.2:c.1368C>T NP_001243243.1:p.Gly456=