Canonical Allele Identifier: CA517464460

Gene: SLC16A2

Linked Data

• MyVariant Identifiers: chrX:g.73641715T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421880T>A , CM000685.2:g.74421880T>A	GRCh38
NC_000023.10:g.73641715T>A , CM000685.1:g.73641715T>A	GRCh37
NC_000023.9:g.73558440T>A	NCBI36
NG_011641.1:g.5631T>A
NG_011641.2:g.5631T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.243T>A MANE Select	ENSP00000465734.1:p.Pro81=
ENST00000587091.5:c.243T>A	ENSP00000465734.1:p.Pro81=
NM_006517.4:c.243T>A	NP_006508.2:p.Pro81=
XM_005262294.1:c.243T>A	XP_005262351.1:p.Pro81=
XM_011531015.1:c.243T>A	XP_011529317.1:p.Pro81=
NM_006517.5:c.243T>A MANE Select	NP_006508.2:p.Pro81=