Canonical Allele Identifier: CA514277425
Gene: SLC5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32500793C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32104806C>T , CM000684.2:g.32104806C>T GRCh38
NC_000022.10:g.32500793C>T , CM000684.1:g.32500793C>T GRCh37
NC_000022.9:g.30830793C>T NCBI36
NG_017045.1:g.66775C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266088.9:c.1686C>T MANE Select ENSP00000266088.4:p.Ser562=
ENST00000266088.8:c.1686C>T ENSP00000266088.4:p.Ser562=
ENST00000543737.2:c.1305C>T ENSP00000444898.1:p.Ser435=
NM_000343.3:c.1686C>T NP_000334.1:p.Ser562=
NM_001256314.1:c.1305C>T NP_001243243.1:p.Ser435=
XR_938173.1:n.591+2032G>A
XR_938174.1:n.486+15049G>A
NM_000343.4:c.1686C>T MANE Select NP_000334.1:p.Ser562=
NM_001256314.2:c.1305C>T NP_001243243.1:p.Ser435=