Canonical Allele Identifier: CA514277437
Gene: SLC5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32500817T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32104830T>G , CM000684.2:g.32104830T>G GRCh38
NC_000022.10:g.32500817T>G , CM000684.1:g.32500817T>G GRCh37
NC_000022.9:g.30830817T>G NCBI36
NG_017045.1:g.66799T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266088.9:c.1710T>G MANE Select ENSP00000266088.4:p.Arg570=
ENST00000266088.8:c.1710T>G ENSP00000266088.4:p.Arg570=
ENST00000543737.2:c.1329T>G ENSP00000444898.1:p.Arg443=
NM_000343.3:c.1710T>G NP_000334.1:p.Arg570=
NM_001256314.1:c.1329T>G NP_001243243.1:p.Arg443=
XR_938173.1:n.591+2008A>C
XR_938174.1:n.486+15025A>C
NM_000343.4:c.1710T>G MANE Select NP_000334.1:p.Arg570=
NM_001256314.2:c.1329T>G NP_001243243.1:p.Arg443=