Canonical Allele Identifier: CA2437472649

Gene: SLC16A2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.289G= MANE Select	ENSP00000465734.1:p.Gly97=
ENST00000636771.1:c.35G=
ENST00000587091.5:c.289G=	ENSP00000465734.1:p.Gly97=
NM_006517.4:c.289G=	NP_006508.2:p.Gly97=
XM_005262294.1:c.289G=	XP_005262351.1:p.Gly97=
XM_011531015.1:c.289G=	XP_011529317.1:p.Gly97=
NM_006517.5:c.289G= MANE Select	NP_006508.2:p.Gly97=