Canonical Allele Identifier: CA381814269

Gene: UCP3

Linked Data

• MyVariant Identifiers: chr11:g.73716789C>T (hg19) ; chr11:g.74005744C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74005744C>T , CM000673.2:g.74005744C>T	GRCh38
NC_000011.9:g.73716789C>T , CM000673.1:g.73716789C>T	GRCh37
NC_000011.8:g.73394437C>T	NCBI36
NG_011515.1:g.8494G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314032.9:c.527G>A MANE Select	ENSP00000323740.4:p.Arg176Lys
ENST00000314032.8:c.527G>A	ENSP00000323740.4:p.Arg176Lys
ENST00000426995.2:c.527G>A	ENSP00000392143.2:p.Arg176Lys
NM_003356.3:c.527G>A	NP_003347.1:p.Arg176Lys
NM_022803.2:c.527G>A	NP_073714.1:p.Arg176Lys
XR_950298.1:n.1768+9710C>T
NM_003356.4:c.527G>A MANE Select	NP_003347.1:p.Arg176Lys
NM_022803.3:c.527G>A	NP_073714.1:p.Arg176Lys