Canonical Allele Identifier: CA411314555
Gene: SLC5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32500792G>C (hg19) chr22:g.32104805G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32104805G>C , CM000684.2:g.32104805G>C GRCh38
NC_000022.10:g.32500792G>C , CM000684.1:g.32500792G>C GRCh37
NC_000022.9:g.30830792G>C NCBI36
NG_017045.1:g.66774G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000266088.9:c.1685G>C MANE Select ENSP00000266088.4:p.Ser562Thr
ENST00000266088.8:c.1685G>C ENSP00000266088.4:p.Ser562Thr
ENST00000543737.2:c.1304G>C ENSP00000444898.1:p.Ser435Thr
NM_000343.3:c.1685G>C NP_000334.1:p.Ser562Thr
NM_001256314.1:c.1304G>C NP_001243243.1:p.Ser435Thr
XR_938173.1:n.591+2033C>G
XR_938174.1:n.486+15050C>G
NM_000343.4:c.1685G>C MANE Select NP_000334.1:p.Ser562Thr
NM_001256314.2:c.1304G>C NP_001243243.1:p.Ser435Thr
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