Canonical Allele Identifier: CA475655822

Gene: UCP2

Linked Data

• MyVariant Identifiers: chr11:g.73689115C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73978070C>A , CM000673.2:g.73978070C>A	GRCh38
NC_000011.9:g.73689115C>A , CM000673.1:g.73689115C>A	GRCh37
NC_000011.8:g.73366763C>A	NCBI36
NG_011478.1:g.9775G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310473.9:c.153G>T	ENSP00000312029.3:p.Val51=
ENST00000663595.2:c.153G>T MANE Select	ENSP00000499695.1:p.Val51=
ENST00000310473.7:c.153G>T	ENSP00000312029.3:p.Val51=
ENST00000536983.5:c.153G>T	ENSP00000441147.1:p.Val51=
ENST00000544615.5:c.72G>T	ENSP00000439951.1:p.Val24=
NM_003355.2:c.153G>T	NP_003346.2:p.Val51=
XM_024448674.1:c.156G>T	XP_024304442.1:p.Val52=
NM_001381943.1:c.153G>T	NP_001368872.1:p.Val51=
NM_001381944.1:c.153G>T	NP_001368873.1:p.Val51=
NM_001381945.1:c.153G>T	NP_001368874.1:p.Val51=
NM_001381947.1:c.153G>T	NP_001368876.1:p.Val51=
NM_001381948.1:c.153G>T	NP_001368877.1:p.Val51=
NM_001381949.1:c.153G>T	NP_001368878.1:p.Val51=
NM_001381950.1:c.153G>T	NP_001368879.1:p.Val51=
NM_003355.3:c.153G>T MANE Select	NP_003346.2:p.Val51=