Canonical Allele Identifier: CA514277452
Gene: SLC5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32500847C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32104860C>A , CM000684.2:g.32104860C>A GRCh38
NC_000022.10:g.32500847C>A , CM000684.1:g.32500847C>A GRCh37
NC_000022.9:g.30830847C>A NCBI36
NG_017045.1:g.66829C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266088.9:c.1740C>A MANE Select ENSP00000266088.4:p.Ile580=
ENST00000266088.8:c.1740C>A ENSP00000266088.4:p.Ile580=
ENST00000543737.2:c.1359C>A ENSP00000444898.1:p.Ile453=
NM_000343.3:c.1740C>A NP_000334.1:p.Ile580=
NM_001256314.1:c.1359C>A NP_001243243.1:p.Ile453=
XR_938173.1:n.591+1978G>T
XR_938174.1:n.486+14995G>T
NM_000343.4:c.1740C>A MANE Select NP_000334.1:p.Ile580=
NM_001256314.2:c.1359C>A NP_001243243.1:p.Ile453=