Canonical Allele Identifier: CA1982686304

Gene: UCP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73978053_73978088delinsGCGCTGGCTGTAGCGCGCACTGGCCCCTGACTTTCT , CM000673.2:g.73978053_73978088delinsGCGCTGGCTGTAGCGCGCACTGGCCCCTGACTTTCT	GRCh38
NC_000011.9:g.73689098_73689133delinsGCGCTGGCTGTAGCGCGCACTGGCCCCTGACTTTCT , CM000673.1:g.73689098_73689133delinsGCGCTGGCTGTAGCGCGCACTGGCCCCTGACTTTCT	GRCh37
NC_000011.8:g.73366746_73366781delinsGCGCTGGCTGTAGCGCGCACTGGCCCCTGACTTTCT	NCBI36
NG_011478.1:g.9757_9792delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000310473.9:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	ENSP00000312029.3:p.Gly45=
ENST00000663595.2:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC MANE Select	ENSP00000499695.1:p.Gly45=
ENST00000310473.7:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	ENSP00000312029.3:p.Gly45=
ENST00000536983.5:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	ENSP00000441147.1:p.Gly45=
ENST00000544615.5:c.54_89delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	ENSP00000439951.1:p.Gly18=
NM_003355.2:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	NP_003346.2:p.Gly45=
XM_024448674.1:c.138_173delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	XP_024304442.1:p.Gly46=
NM_001381943.1:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	NP_001368872.1:p.Gly45=
NM_001381944.1:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	NP_001368873.1:p.Gly45=
NM_001381945.1:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	NP_001368874.1:p.Gly45=
NM_001381947.1:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	NP_001368876.1:p.Gly45=
NM_001381948.1:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	NP_001368877.1:p.Gly45=
NM_001381949.1:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	NP_001368878.1:p.Gly45=
NM_001381950.1:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC	NP_001368879.1:p.Gly45=
NM_003355.3:c.135_170delinsAGAAAGTCAGGGGCCAGTGCGCGCTACAGCCAGCGC MANE Select	NP_003346.2:p.Gly45=