Canonical Allele Identifier: CA1189549801
Gene: SLC16A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112917624_112917626delinsCTG , CM000663.2:g.112917624_112917626delinsCTG GRCh38
NC_000001.10:g.113460246_113460248delinsCTG , CM000663.1:g.113460246_113460248delinsCTG GRCh37
NC_000001.9:g.113261769_113261771delinsCTG NCBI36
NG_015880.2:g.43303_43305delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369626.8:c.780_782delinsCAG MANE Select ENSP00000358640.4:p.His260=
ENST00000429288.2:c.780_782delinsCAG ENSP00000397106.2:p.His260=
ENST00000443580.6:c.780_782delinsCAG ENSP00000399104.2:p.His260=
ENST00000458229.6:c.780_782delinsCAG ENSP00000416167.2:p.His260=
ENST00000679803.1:c.780_782delinsCAG ENSP00000505879.1:p.His260=
ENST00000679846.1:n.1697_1699delinsCAG
ENST00000369626.7:c.780_782delinsCAG ENSP00000358640.3:p.His260=
ENST00000443580.5:c.780_782delinsCAG ENSP00000399104.1:p.His260=
ENST00000458229.5:c.780_782delinsCAG ENSP00000416167.1:p.His260=
ENST00000538576.5:c.780_782delinsCAG ENSP00000441065.1:p.His260=
NM_001166496.1:c.780_782delinsCAG NP_001159968.1:p.His260=
NM_003051.3:c.780_782delinsCAG NP_003042.3:p.His260=
XM_011542026.1:c.780_782delinsCAG XP_011540328.1:p.His260=
XM_011542027.1:c.780_782delinsCAG XP_011540329.1:p.His260=
NM_003051.4:c.780_782delinsCAG MANE Select NP_003042.3:p.His260=
NM_001166496.2:c.780_782delinsCAG NP_001159968.1:p.His260=