Canonical Allele Identifier: CA381812025

Gene: UCP2

Linked Data

• MyVariant Identifiers: chr11:g.73689149G>A (hg19) ; chr11:g.73978104G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73978104G>A , CM000673.2:g.73978104G>A	GRCh38
NC_000011.9:g.73689149G>A , CM000673.1:g.73689149G>A	GRCh37
NC_000011.8:g.73366797G>A	NCBI36
NG_011478.1:g.9741C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310473.9:c.127-8C>T	ENSP00000312029.3:n.127-8C>T
ENST00000663595.2:c.127-8C>T MANE Select	ENSP00000499695.1:n.127-8C>T
ENST00000310473.7:c.127-8C>T	ENSP00000312029.3:n.127-8C>T
ENST00000536983.5:c.127-8C>T	ENSP00000441147.1:n.127-8C>T
ENST00000544615.5:c.38C>T	ENSP00000439951.1:p.Ala13Val
NM_003355.2:c.127-8C>T	NP_003346.2:n.127-8C>T
XM_024448674.1:c.122C>T	XP_024304442.1:p.Ala41Val
NM_001381943.1:c.127-8C>T	NP_001368872.1:n.127-8C>T
NM_001381944.1:c.127-8C>T	NP_001368873.1:n.127-8C>T
NM_001381945.1:c.127-8C>T	NP_001368874.1:n.127-8C>T
NM_001381947.1:c.127-8C>T	NP_001368876.1:n.127-8C>T
NM_001381948.1:c.127-8C>T	NP_001368877.1:n.127-8C>T
NM_001381949.1:c.127-8C>T	NP_001368878.1:n.127-8C>T
NM_001381950.1:c.127-8C>T	NP_001368879.1:n.127-8C>T
NM_003355.3:c.127-8C>T MANE Select	NP_003346.2:n.127-8C>T