Canonical Allele Identifier: CA1982686317

Gene: UCP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73978069G= , CM000673.2:g.73978069G=	GRCh38
NC_000011.9:g.73689114G= , CM000673.1:g.73689114G=	GRCh37
NC_000011.8:g.73366762G=	NCBI36
NG_011478.1:g.9776C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310473.9:c.154C=	ENSP00000312029.3:p.Arg52=
ENST00000663595.2:c.154C= MANE Select	ENSP00000499695.1:p.Arg52=
ENST00000310473.7:c.154C=	ENSP00000312029.3:p.Arg52=
ENST00000536983.5:c.154C=	ENSP00000441147.1:p.Arg52=
ENST00000544615.5:c.73C=	ENSP00000439951.1:p.Arg25=
NM_003355.2:c.154C=	NP_003346.2:p.Arg52=
XM_024448674.1:c.157C=	XP_024304442.1:p.Arg53=
NM_001381943.1:c.154C=	NP_001368872.1:p.Arg52=
NM_001381944.1:c.154C=	NP_001368873.1:p.Arg52=
NM_001381945.1:c.154C=	NP_001368874.1:p.Arg52=
NM_001381947.1:c.154C=	NP_001368876.1:p.Arg52=
NM_001381948.1:c.154C=	NP_001368877.1:p.Arg52=
NM_001381949.1:c.154C=	NP_001368878.1:p.Arg52=
NM_001381950.1:c.154C=	NP_001368879.1:p.Arg52=
NM_003355.3:c.154C= MANE Select	NP_003346.2:p.Arg52=