Canonical Allele Identifier: CA1239233173
Gene: POMC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25167149_25167150delinsAG , CM000664.2:g.25167149_25167150delinsAG GRCh38
NC_000002.11:g.25390018_25390019delinsAG , CM000664.1:g.25390018_25390019delinsAG GRCh37
NC_000002.10:g.25243522_25243523delinsAG NCBI36
NG_008997.1:g.6541_6542delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.-21+1348_-21+1349delinsCT MANE Select ENSP00000379170.2:n.-21+1348_-21+1349deli...
ENST00000264708.7:c.-101+1348_-101+1349delinsCT ENSP00000264708.3:n.-101+1348_-101+1349de...
ENST00000380794.5:c.-71+1348_-71+1349delinsCT ENSP00000370171.1:n.-71+1348_-71+1349deli...
ENST00000395826.6:c.-21+1348_-21+1349delinsCT ENSP00000379170.2:n.-21+1348_-21+1349deli...
ENST00000405623.5:c.-51+1348_-51+1349delinsCT ENSP00000384092.1:n.-51+1348_-51+1349deli...
ENST00000449220.1:c.-71+1348_-71+1349delinsCT ENSP00000387993.1:n.-71+1348_-71+1349deli...
NM_000939.2:c.-21+1348_-21+1349delinsCT NP_000930.1:n.-21+1348_-21+1349delinsCT
NM_001035256.1:c.-71+1348_-71+1349delinsCT NP_001030333.1:n.-71+1348_-71+1349delinsC...
XM_011532917.1:c.-51+1348_-51+1349delinsCT XP_011531219.1:n.-51+1348_-51+1349delinsC...
NM_000939.3:c.-21+1348_-21+1349delinsCT NP_000930.1:n.-21+1348_-21+1349delinsCT
NM_001035256.2:c.-71+1348_-71+1349delinsCT NP_001030333.1:n.-71+1348_-71+1349delinsC...
NM_001319204.1:c.-101+1348_-101+1349delinsCT NP_001306133.1:n.-101+1348_-101+1349delin...
NM_001319205.1:c.-51+1348_-51+1349delinsCT NP_001306134.1:n.-51+1348_-51+1349delinsC...
NM_000939.4:c.-21+1348_-21+1349delinsCT MANE Select NP_000930.1:n.-21+1348_-21+1349delinsCT
NM_001319204.2:c.-101+1348_-101+1349delinsCT NP_001306133.1:n.-101+1348_-101+1349delin...
NM_001319205.2:c.-51+1348_-51+1349delinsCT NP_001306134.1:n.-51+1348_-51+1349delinsC...
NM_001035256.3:c.-71+1348_-71+1349delinsCT NP_001030333.1:n.-71+1348_-71+1349delinsC...