Canonical Allele Identifier: CA413656168

Gene: SLC16A2

Linked Data

• MyVariant Identifiers: chrX:g.73641761G>C (hg19) ; chrX:g.74421926G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421926G>C , CM000685.2:g.74421926G>C	GRCh38
NC_000023.10:g.73641761G>C , CM000685.1:g.73641761G>C	GRCh37
NC_000023.9:g.73558486G>C	NCBI36
NG_011641.1:g.5677G>C
NG_011641.2:g.5677G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.289G>C MANE Select	ENSP00000465734.1:p.Gly97Arg
ENST00000636771.1:c.35G>C
ENST00000587091.5:c.289G>C	ENSP00000465734.1:p.Gly97Arg
NM_006517.4:c.289G>C	NP_006508.2:p.Gly97Arg
XM_005262294.1:c.289G>C	XP_005262351.1:p.Gly97Arg
XM_011531015.1:c.289G>C	XP_011529317.1:p.Gly97Arg
NM_006517.5:c.289G>C MANE Select	NP_006508.2:p.Gly97Arg