Canonical Allele Identifier: CA381814337

Gene: UCP3

Linked Data

• MyVariant Identifiers: chr11:g.73716801T>G (hg19) ; chr11:g.74005756T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74005756T>G , CM000673.2:g.74005756T>G	GRCh38
NC_000011.9:g.73716801T>G , CM000673.1:g.73716801T>G	GRCh37
NC_000011.8:g.73394449T>G	NCBI36
NG_011515.1:g.8482A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314032.9:c.515A>C MANE Select	ENSP00000323740.4:p.Glu172Ala
ENST00000314032.8:c.515A>C	ENSP00000323740.4:p.Glu172Ala
ENST00000426995.2:c.515A>C	ENSP00000392143.2:p.Glu172Ala
NM_003356.3:c.515A>C	NP_003347.1:p.Glu172Ala
NM_022803.2:c.515A>C	NP_073714.1:p.Glu172Ala
XR_950298.1:n.1768+9722T>G
NM_003356.4:c.515A>C MANE Select	NP_003347.1:p.Glu172Ala
NM_022803.3:c.515A>C	NP_073714.1:p.Glu172Ala