Canonical Allele Identifier: CA1145931737

Gene: SLC16A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.112917726T= , CM000663.2:g.112917726T=	GRCh38
NC_000001.10:g.113460348T= , CM000663.1:g.113460348T=	GRCh37
NC_000001.9:g.113261871T=	NCBI36
NG_015880.2:g.43203A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369626.8:c.680A= MANE Select	ENSP00000358640.4:p.His227=
ENST00000429288.2:c.680A=	ENSP00000397106.2:p.His227=
ENST00000443580.6:c.680A=	ENSP00000399104.2:p.His227=
ENST00000458229.6:c.680A=	ENSP00000416167.2:p.His227=
ENST00000679803.1:c.680A=	ENSP00000505879.1:p.His227=
ENST00000679846.1:n.1597A=
ENST00000369626.7:c.680A=	ENSP00000358640.3:p.His227=
ENST00000443580.5:c.680A=	ENSP00000399104.1:p.His227=
ENST00000458229.5:c.680A=	ENSP00000416167.1:p.His227=
ENST00000538576.5:c.680A=	ENSP00000441065.1:p.His227=
NM_001166496.1:c.680A=	NP_001159968.1:p.His227=
NM_003051.3:c.680A=	NP_003042.3:p.His227=
XM_011542026.1:c.680A=	XP_011540328.1:p.His227=
XM_011542027.1:c.680A=	XP_011540329.1:p.His227=
NM_003051.4:c.680A= MANE Select	NP_003042.3:p.His227=
NM_001166496.2:c.680A=	NP_001159968.1:p.His227=