Canonical Allele Identifier: CA1239231286
Gene: POMC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25164332_25164334delinsAGG , CM000664.2:g.25164332_25164334delinsAGG GRCh38
NC_000002.11:g.25387201_25387203delinsAGG , CM000664.1:g.25387201_25387203delinsAGG GRCh37
NC_000002.10:g.25240705_25240707delinsAGG NCBI36
NG_008997.1:g.9357_9359delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395826.7:c.132+307_132+309delinsCCT MANE Select ENSP00000379170.2:n.132+307_132+309delinsCCT
ENST00000264708.7:c.132+307_132+309delinsCCT ENSP00000264708.3:n.132+307_132+309delinsCCT
ENST00000380794.5:c.132+307_132+309delinsCCT ENSP00000370171.1:n.132+307_132+309delinsCCT
ENST00000395826.6:c.132+307_132+309delinsCCT ENSP00000379170.2:n.132+307_132+309delinsCCT
ENST00000405623.5:c.132+307_132+309delinsCCT ENSP00000384092.1:n.132+307_132+309delinsCCT
ENST00000449220.1:c.132+307_132+309delinsCCT ENSP00000387993.1:n.132+307_132+309delinsCCT
NM_000939.2:c.132+307_132+309delinsCCT NP_000930.1:n.132+307_132+309delinsCCT
NM_001035256.1:c.132+307_132+309delinsCCT NP_001030333.1:n.132+307_132+309delinsCCT
XM_011532917.1:c.132+307_132+309delinsCCT XP_011531219.1:n.132+307_132+309delinsCCT
NM_000939.3:c.132+307_132+309delinsCCT NP_000930.1:n.132+307_132+309delinsCCT
NM_001035256.2:c.132+307_132+309delinsCCT NP_001030333.1:n.132+307_132+309delinsCCT
NM_001319204.1:c.132+307_132+309delinsCCT NP_001306133.1:n.132+307_132+309delinsCCT
NM_001319205.1:c.132+307_132+309delinsCCT NP_001306134.1:n.132+307_132+309delinsCCT
NM_000939.4:c.132+307_132+309delinsCCT MANE Select NP_000930.1:n.132+307_132+309delinsCCT
NM_001319204.2:c.132+307_132+309delinsCCT NP_001306133.1:n.132+307_132+309delinsCCT
NM_001319205.2:c.132+307_132+309delinsCCT NP_001306134.1:n.132+307_132+309delinsCCT
NM_001035256.3:c.132+307_132+309delinsCCT NP_001030333.1:n.132+307_132+309delinsCCT