Canonical Allele Identifier: CA1982698706
Gene: UCP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74005743_74005745delinsCCT , CM000673.2:g.74005743_74005745delinsCCT GRCh38
NC_000011.9:g.73716788_73716790delinsCCT , CM000673.1:g.73716788_73716790delinsCCT GRCh37
NC_000011.8:g.73394436_73394438delinsCCT NCBI36
NG_011515.1:g.8493_8495delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000314032.9:c.526_528delinsAGG MANE Select ENSP00000323740.4:p.Arg176=
ENST00000314032.8:c.526_528delinsAGG ENSP00000323740.4:p.Arg176=
ENST00000426995.2:c.526_528delinsAGG ENSP00000392143.2:p.Arg176=
NM_003356.3:c.526_528delinsAGG NP_003347.1:p.Arg176=
NM_022803.2:c.526_528delinsAGG NP_073714.1:p.Arg176=
XR_950298.1:n.1768+9709_1768+9711delinsCCT
NM_003356.4:c.526_528delinsAGG MANE Select NP_003347.1:p.Arg176=
NM_022803.3:c.526_528delinsAGG NP_073714.1:p.Arg176=
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