Canonical Allele Identifier: CA411314832
Gene: SLC5A1 HGNC NCBI

Linked Data

dbSNP Id: rs1226808441

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32104867G>C , CM000684.2:g.32104867G>C GRCh38
NC_000022.10:g.32500854G>C , CM000684.1:g.32500854G>C GRCh37
NC_000022.9:g.30830854G>C NCBI36
NG_017045.1:g.66836G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266088.9:c.1747G>C MANE Select ENSP00000266088.4:p.Gly583Arg
ENST00000266088.8:c.1747G>C ENSP00000266088.4:p.Gly583Arg
ENST00000543737.2:c.1366G>C ENSP00000444898.1:p.Gly456Arg
NM_000343.3:c.1747G>C NP_000334.1:p.Gly583Arg
NM_001256314.1:c.1366G>C NP_001243243.1:p.Gly456Arg
XR_938173.1:n.591+1971C>G
XR_938174.1:n.486+14988C>G
NM_000343.4:c.1747G>C MANE Select NP_000334.1:p.Gly583Arg
NM_001256314.2:c.1366G>C NP_001243243.1:p.Gly456Arg