Canonical Allele Identifier: CA411314471

Gene: SLC5A1

Linked Data

• dbSNP Id: rs201078847
• MyVariant Identifiers: chr22:g.32500778C>A (hg19) ; chr22:g.32104791C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32104791C>A , CM000684.2:g.32104791C>A	GRCh38
NC_000022.10:g.32500778C>A , CM000684.1:g.32500778C>A	GRCh37
NC_000022.9:g.30830778C>A	NCBI36
NG_017045.1:g.66760C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266088.9:c.1671C>A MANE Select	ENSP00000266088.4:p.Tyr557Ter
ENST00000266088.8:c.1671C>A	ENSP00000266088.4:p.Tyr557Ter
ENST00000543737.2:c.1290C>A	ENSP00000444898.1:p.Tyr430Ter
NM_000343.3:c.1671C>A	NP_000334.1:p.Tyr557Ter
NM_001256314.1:c.1290C>A	NP_001243243.1:p.Tyr430Ter
XR_938173.1:n.591+2047G>T
XR_938174.1:n.486+15064G>T
NM_000343.4:c.1671C>A MANE Select	NP_000334.1:p.Tyr557Ter
NM_001256314.2:c.1290C>A	NP_001243243.1:p.Tyr430Ter