Canonical Allele Identifier: CA2437472638

Gene: SLC16A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421904G= , CM000685.2:g.74421904G=	GRCh38
NC_000023.10:g.73641739G= , CM000685.1:g.73641739G=	GRCh37
NC_000023.9:g.73558464G=	NCBI36
NG_011641.1:g.5655G=
NG_011641.2:g.5655G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.267G= MANE Select	ENSP00000465734.1:p.Ala89=
ENST00000636771.1:c.13G=
ENST00000587091.5:c.267G=	ENSP00000465734.1:p.Ala89=
NM_006517.4:c.267G=	NP_006508.2:p.Ala89=
XM_005262294.1:c.267G=	XP_005262351.1:p.Ala89=
XM_011531015.1:c.267G=	XP_011529317.1:p.Ala89=
NM_006517.5:c.267G= MANE Select	NP_006508.2:p.Ala89=