Canonical Allele Identifier: CA381814317

Gene: UCP3

Linked Data

• MyVariant Identifiers: chr11:g.73716798T>A (hg19) ; chr11:g.74005753T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74005753T>A , CM000673.2:g.74005753T>A	GRCh38
NC_000011.9:g.73716798T>A , CM000673.1:g.73716798T>A	GRCh37
NC_000011.8:g.73394446T>A	NCBI36
NG_011515.1:g.8485A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314032.9:c.518A>T MANE Select	ENSP00000323740.4:p.Glu173Val
ENST00000314032.8:c.518A>T	ENSP00000323740.4:p.Glu173Val
ENST00000426995.2:c.518A>T	ENSP00000392143.2:p.Glu173Val
NM_003356.3:c.518A>T	NP_003347.1:p.Glu173Val
NM_022803.2:c.518A>T	NP_073714.1:p.Glu173Val
XR_950298.1:n.1768+9719T>A
NM_003356.4:c.518A>T MANE Select	NP_003347.1:p.Glu173Val
NM_022803.3:c.518A>T	NP_073714.1:p.Glu173Val