Canonical Allele Identifier: CA2437472610

Gene: SLC16A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421844C= , CM000685.2:g.74421844C=	GRCh38
NC_000023.10:g.73641679C= , CM000685.1:g.73641679C=	GRCh37
NC_000023.9:g.73558404C=	NCBI36
NG_011641.1:g.5595C=
NG_011641.2:g.5595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.207C= MANE Select	ENSP00000465734.1:p.Phe69=
ENST00000587091.5:c.207C=	ENSP00000465734.1:p.Phe69=
NM_006517.4:c.207C=	NP_006508.2:p.Phe69=
XM_005262294.1:c.207C=	XP_005262351.1:p.Phe69=
XM_011531015.1:c.207C=	XP_011529317.1:p.Phe69=
NM_006517.5:c.207C= MANE Select	NP_006508.2:p.Phe69=