Canonical Allele Identifier: CA381814324

Gene: UCP3

Linked Data

• MyVariant Identifiers: chr11:g.73716799C>A (hg19) ; chr11:g.74005754C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74005754C>A , CM000673.2:g.74005754C>A	GRCh38
NC_000011.9:g.73716799C>A , CM000673.1:g.73716799C>A	GRCh37
NC_000011.8:g.73394447C>A	NCBI36
NG_011515.1:g.8484G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314032.9:c.517G>T MANE Select	ENSP00000323740.4:p.Glu173Ter
ENST00000314032.8:c.517G>T	ENSP00000323740.4:p.Glu173Ter
ENST00000426995.2:c.517G>T	ENSP00000392143.2:p.Glu173Ter
NM_003356.3:c.517G>T	NP_003347.1:p.Glu173Ter
NM_022803.2:c.517G>T	NP_073714.1:p.Glu173Ter
XR_950298.1:n.1768+9720C>A
NM_003356.4:c.517G>T MANE Select	NP_003347.1:p.Glu173Ter
NM_022803.3:c.517G>T	NP_073714.1:p.Glu173Ter