Canonical Allele Identifier: CA2437472655

Gene: SLC16A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421950T= , CM000685.2:g.74421950T=	GRCh38
NC_000023.10:g.73641785T= , CM000685.1:g.73641785T=	GRCh37
NC_000023.9:g.73558510T=	NCBI36
NG_011641.1:g.5701T=
NG_011641.2:g.5701T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.313T= MANE Select	ENSP00000465734.1:p.Phe105=
ENST00000636771.1:c.59T=
ENST00000587091.5:c.313T=	ENSP00000465734.1:p.Phe105=
NM_006517.4:c.313T=	NP_006508.2:p.Phe105=
XM_005262294.1:c.313T=	XP_005262351.1:p.Phe105=
XM_011531015.1:c.313T=	XP_011529317.1:p.Phe105=
NM_006517.5:c.313T= MANE Select	NP_006508.2:p.Phe105=