Canonical Allele Identifier: CA2647176200

Gene: SLC16A1

Linked Data

• gnomAD v4: 1-112913870-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.112913870T>C , CM000663.2:g.112913870T>C	GRCh38
NC_000001.10:g.113456492T>C , CM000663.1:g.113456492T>C	GRCh37
NC_000001.9:g.113258015T>C	NCBI36
NG_015880.2:g.47059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369626.8:c.*21A>G MANE Select	ENSP00000358640.4:n.*21A>G
ENST00000429288.2:c.*21A>G	ENSP00000397106.2:n.*21A>G
ENST00000443580.6:c.*21A>G	ENSP00000399104.2:n.*21A>G
ENST00000458229.6:c.*21A>G	ENSP00000416167.2:n.*21A>G
ENST00000679803.1:c.*21A>G	ENSP00000505879.1:n.*21A>G
ENST00000369626.7:c.*21A>G	ENSP00000358640.3:n.*21A>G
ENST00000538576.5:c.*21A>G	ENSP00000441065.1:n.*21A>G
NM_001166496.1:c.*21A>G	NP_001159968.1:n.*21A>G
NM_003051.3:c.*21A>G	NP_003042.3:n.*21A>G
XM_011542026.1:c.*21A>G	XP_011540328.1:n.*21A>G
XM_011542027.1:c.*21A>G	XP_011540329.1:n.*21A>G
NM_003051.4:c.*21A>G MANE Select	NP_003042.3:n.*21A>G
NM_001166496.2:c.*21A>G	NP_001159968.1:n.*21A>G