Canonical Allele Identifier: CA381811789

Gene: UCP2

Linked Data

• MyVariant Identifiers: chr11:g.73689029T>G (hg19) ; chr11:g.73977984T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73977984T>G , CM000673.2:g.73977984T>G	GRCh38
NC_000011.9:g.73689029T>G , CM000673.1:g.73689029T>G	GRCh37
NC_000011.8:g.73366677T>G	NCBI36
NG_011478.1:g.9861A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310473.9:c.239A>C	ENSP00000312029.3:p.Asn80Thr
ENST00000663595.2:c.239A>C MANE Select	ENSP00000499695.1:p.Asn80Thr
ENST00000310473.7:c.239A>C	ENSP00000312029.3:p.Asn80Thr
ENST00000536983.5:c.239A>C	ENSP00000441147.1:p.Asn80Thr
ENST00000544615.5:c.158A>C	ENSP00000439951.1:p.Asn53Thr
NM_003355.2:c.239A>C	NP_003346.2:p.Asn80Thr
XM_024448674.1:c.242A>C	XP_024304442.1:p.Asn81Thr
NM_001381943.1:c.239A>C	NP_001368872.1:p.Asn80Thr
NM_001381944.1:c.239A>C	NP_001368873.1:p.Asn80Thr
NM_001381945.1:c.239A>C	NP_001368874.1:p.Asn80Thr
NM_001381947.1:c.239A>C	NP_001368876.1:p.Asn80Thr
NM_001381948.1:c.239A>C	NP_001368877.1:p.Asn80Thr
NM_001381949.1:c.239A>C	NP_001368878.1:p.Asn80Thr
NM_001381950.1:c.239A>C	NP_001368879.1:p.Asn80Thr
NM_003355.3:c.239A>C MANE Select	NP_003346.2:p.Asn80Thr