Canonical Allele Identifier: CA381814343

Gene: UCP3

Linked Data

• MyVariant Identifiers: chr11:g.73716802C>T (hg19) ; chr11:g.74005757C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74005757C>T , CM000673.2:g.74005757C>T	GRCh38
NC_000011.9:g.73716802C>T , CM000673.1:g.73716802C>T	GRCh37
NC_000011.8:g.73394450C>T	NCBI36
NG_011515.1:g.8481G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314032.9:c.514G>A MANE Select	ENSP00000323740.4:p.Glu172Lys
ENST00000314032.8:c.514G>A	ENSP00000323740.4:p.Glu172Lys
ENST00000426995.2:c.514G>A	ENSP00000392143.2:p.Glu172Lys
NM_003356.3:c.514G>A	NP_003347.1:p.Glu172Lys
NM_022803.2:c.514G>A	NP_073714.1:p.Glu172Lys
XR_950298.1:n.1768+9723C>T
NM_003356.4:c.514G>A MANE Select	NP_003347.1:p.Glu172Lys
NM_022803.3:c.514G>A	NP_073714.1:p.Glu172Lys