Canonical Allele Identifier: CA531760855
Gene: POMC HGNC NCBI

Linked Data

ClinVar Variation Id: 2167896
ClinVar RCV Id: RCV003100213
dbSNP Id: rs10654394

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25161607_25161608insCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGC , CM000664.2:g.25161607_25161608insCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGC GRCh38
NC_000002.11:g.25384476_25384477insCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGC , CM000664.1:g.25384476_25384477insCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGC GRCh37
NC_000002.10:g.25237980_25237981insCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGC NCBI36
NG_008997.1:g.12103_12104insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC MANE Select ENSP00000379170.2:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGl...
ENST00000264708.7:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC ENSP00000264708.3:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGl...
ENST00000380794.5:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC ENSP00000370171.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGl...
ENST00000395826.6:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC ENSP00000379170.2:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGl...
ENST00000405623.5:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC ENSP00000384092.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGl...
ENST00000449220.1:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC ENSP00000387993.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGl...
NM_000939.2:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_000930.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySerSe...
NM_001035256.1:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_001030333.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySe...
XM_011532917.1:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC XP_011531219.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySe...
NM_000939.3:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_000930.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySerSe...
NM_001035256.2:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_001030333.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySe...
NM_001319204.1:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_001306133.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySe...
NM_001319205.1:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_001306134.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySe...
NM_000939.4:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC MANE Select NP_000930.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySerSe...
NM_001319204.2:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_001306133.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySe...
NM_001319205.2:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_001306134.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySe...
NM_001035256.3:c.297_298insAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGC NP_001030333.1:p.Gly99_Ala100insSerSerGlySerSerGlySerSerGlySe...