Canonical Allele Identifier: CA411314623
Gene: SLC5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32500807A>C (hg19) chr22:g.32104820A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32104820A>C , CM000684.2:g.32104820A>C GRCh38
NC_000022.10:g.32500807A>C , CM000684.1:g.32500807A>C GRCh37
NC_000022.9:g.30830807A>C NCBI36
NG_017045.1:g.66789A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266088.9:c.1700A>C MANE Select ENSP00000266088.4:p.Lys567Thr
ENST00000266088.8:c.1700A>C ENSP00000266088.4:p.Lys567Thr
ENST00000543737.2:c.1319A>C ENSP00000444898.1:p.Lys440Thr
NM_000343.3:c.1700A>C NP_000334.1:p.Lys567Thr
NM_001256314.1:c.1319A>C NP_001243243.1:p.Lys440Thr
XR_938173.1:n.591+2018T>G
XR_938174.1:n.486+15035T>G
NM_000343.4:c.1700A>C MANE Select NP_000334.1:p.Lys567Thr
NM_001256314.2:c.1319A>C NP_001243243.1:p.Lys440Thr
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