Canonical Allele Identifier: CA2745088333
Gene: SLC16A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112917723del , CM000663.2:g.112917723del GRCh38
NC_000001.10:g.113460345del , CM000663.1:g.113460345del GRCh37
NC_000001.9:g.113261868del NCBI36
NG_015880.2:g.43206del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369626.8:c.683del MANE Select ENSP00000358640.4:p.Asp228ValfsTer28
ENST00000429288.2:c.683del ENSP00000397106.2:p.Asp228ValfsTer28
ENST00000443580.6:c.683del ENSP00000399104.2:p.Asp228ValfsTer28
ENST00000458229.6:c.683del ENSP00000416167.2:p.Asp228ValfsTer28
ENST00000679803.1:c.683del ENSP00000505879.1:p.Asp228ValfsTer28
ENST00000679846.1:n.1600del
ENST00000369626.7:c.683del ENSP00000358640.3:p.Asp228ValfsTer28
ENST00000443580.5:c.683del ENSP00000399104.1:p.Asp228ValfsTer28
ENST00000458229.5:c.683del ENSP00000416167.1:p.Asp228ValfsTer28
ENST00000538576.5:c.683del ENSP00000441065.1:p.Asp228ValfsTer28
NM_001166496.1:c.683del NP_001159968.1:p.Asp228ValfsTer28
NM_003051.3:c.683del NP_003042.3:p.Asp228ValfsTer28
XM_011542026.1:c.683del XP_011540328.1:p.Asp228ValfsTer28
XM_011542027.1:c.683del XP_011540329.1:p.Asp228ValfsTer28
NM_003051.4:c.683del MANE Select NP_003042.3:p.Asp228ValfsTer28
NM_001166496.2:c.683del NP_001159968.1:p.Asp228ValfsTer28