Canonical Allele Identifier: CA2647176143

Gene: SLC16A1

Linked Data

• gnomAD v4: 1-112913757-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.112913757A>G , CM000663.2:g.112913757A>G	GRCh38
NC_000001.10:g.113456379A>G , CM000663.1:g.113456379A>G	GRCh37
NC_000001.9:g.113257902A>G	NCBI36
NG_015880.2:g.47172T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369626.8:c.*134T>C MANE Select	ENSP00000358640.4:n.*134T>C
ENST00000429288.2:c.*134T>C	ENSP00000397106.2:n.*134T>C
ENST00000443580.6:c.*134T>C	ENSP00000399104.2:n.*134T>C
ENST00000458229.6:c.*134T>C	ENSP00000416167.2:n.*134T>C
ENST00000679803.1:c.*134T>C	ENSP00000505879.1:n.*134T>C
ENST00000369626.7:c.*134T>C	ENSP00000358640.3:n.*134T>C
ENST00000538576.5:c.*134T>C	ENSP00000441065.1:n.*134T>C
NM_001166496.1:c.*134T>C	NP_001159968.1:n.*134T>C
NM_003051.3:c.*134T>C	NP_003042.3:n.*134T>C
XM_011542026.1:c.*134T>C	XP_011540328.1:n.*134T>C
XM_011542027.1:c.*134T>C	XP_011540329.1:n.*134T>C
NM_003051.4:c.*134T>C MANE Select	NP_003042.3:n.*134T>C
NM_001166496.2:c.*134T>C	NP_001159968.1:n.*134T>C