Canonical Allele Identifier: CA341828142
Gene: SLC16A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112917586A>C , CM000663.2:g.112917586A>C GRCh38
NC_000001.10:g.113460208A>C , CM000663.1:g.113460208A>C GRCh37
NC_000001.9:g.113261731A>C NCBI36
NG_015880.2:g.43343T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369626.8:c.820T>G MANE Select ENSP00000358640.4:p.Phe274Val
ENST00000429288.2:c.820T>G ENSP00000397106.2:p.Phe274Val
ENST00000443580.6:c.820T>G ENSP00000399104.2:p.Phe274Val
ENST00000458229.6:c.820T>G ENSP00000416167.2:p.Phe274Val
ENST00000679803.1:c.820T>G ENSP00000505879.1:p.Phe274Val
ENST00000679846.1:n.1737T>G
ENST00000369626.7:c.820T>G ENSP00000358640.3:p.Phe274Val
ENST00000443580.5:c.820T>G ENSP00000399104.1:p.Phe274Val
ENST00000458229.5:c.820T>G ENSP00000416167.1:p.Phe274Val
ENST00000538576.5:c.820T>G ENSP00000441065.1:p.Phe274Val
NM_001166496.1:c.820T>G NP_001159968.1:p.Phe274Val
NM_003051.3:c.820T>G NP_003042.3:p.Phe274Val
XM_011542026.1:c.820T>G XP_011540328.1:p.Phe274Val
XM_011542027.1:c.820T>G XP_011540329.1:p.Phe274Val
NM_003051.4:c.820T>G MANE Select NP_003042.3:p.Phe274Val
NM_001166496.2:c.820T>G NP_001159968.1:p.Phe274Val