Canonical Allele Identifier: CA475873519

Gene: UCP3

Linked Data

• MyVariant Identifiers: chr11:g.73716800C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74005755C>T , CM000673.2:g.74005755C>T	GRCh38
NC_000011.9:g.73716800C>T , CM000673.1:g.73716800C>T	GRCh37
NC_000011.8:g.73394448C>T	NCBI36
NG_011515.1:g.8483G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314032.9:c.516G>A MANE Select	ENSP00000323740.4:p.Glu172=
ENST00000314032.8:c.516G>A	ENSP00000323740.4:p.Glu172=
ENST00000426995.2:c.516G>A	ENSP00000392143.2:p.Glu172=
NM_003356.3:c.516G>A	NP_003347.1:p.Glu172=
NM_022803.2:c.516G>A	NP_073714.1:p.Glu172=
XR_950298.1:n.1768+9721C>T
NM_003356.4:c.516G>A MANE Select	NP_003347.1:p.Glu172=
NM_022803.3:c.516G>A	NP_073714.1:p.Glu172=