Canonical Allele Identifier: CA413656163

Gene: SLC16A2

Linked Data

• MyVariant Identifiers: chrX:g.73641759A>T (hg19) ; chrX:g.74421924A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421924A>T , CM000685.2:g.74421924A>T	GRCh38
NC_000023.10:g.73641759A>T , CM000685.1:g.73641759A>T	GRCh37
NC_000023.9:g.73558484A>T	NCBI36
NG_011641.1:g.5675A>T
NG_011641.2:g.5675A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.287A>T MANE Select	ENSP00000465734.1:p.Glu96Val
ENST00000636771.1:c.33A>T
ENST00000587091.5:c.287A>T	ENSP00000465734.1:p.Glu96Val
NM_006517.4:c.287A>T	NP_006508.2:p.Glu96Val
XM_005262294.1:c.287A>T	XP_005262351.1:p.Glu96Val
XM_011531015.1:c.287A>T	XP_011529317.1:p.Glu96Val
NM_006517.5:c.287A>T MANE Select	NP_006508.2:p.Glu96Val