Canonical Allele Identifier: CA411302822
Community Standard Title: NM_000343.4(SLC5A1):c.625G>C (p.Val209Leu)
Gene: SLC5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32083115G>C , CM000684.2:g.32083115G>C GRCh38
NC_000022.10:g.32479102G>C , CM000684.1:g.32479102G>C GRCh37
NC_000022.9:g.30809102G>C NCBI36
NG_017045.1:g.45084G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000343.4:c.625G>C MANE Select NP_000334.1:p.Val209Leu
ENST00000266088.9:c.625G>C MANE Select ENSP00000266088.4:p.Val209Leu
NM_000343.3:c.625G>C NP_000334.1:p.Val209Leu
NM_001256314.1:c.244G>C NP_001243243.1:p.Val82Leu
NM_001256314.2:c.244G>C NP_001243243.1:p.Val82Leu
ENST00000266088.8:c.625G>C ENSP00000266088.4:p.Val209Leu
ENST00000486394.1:n.65G>C
ENST00000543737.2:c.244G>C ENSP00000444898.1:p.Val82Leu
XM_011530331.1:c.625G>C XP_011528633.1:p.Val209Leu
XR_938173.1:n.592-14312C>G
XR_938174.1:n.487-14312C>G