Canonical Allele Identifier: CA1239233649
Gene: POMC HGNC NCBI

Linked Data

dbSNP Id: rs1671621776

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25168168_25168169insG , CM000664.2:g.25168168_25168169insG GRCh38
NC_000002.11:g.25391037_25391038insG , CM000664.1:g.25391037_25391038insG GRCh37
NC_000002.10:g.25244541_25244542insG NCBI36
NG_008997.1:g.5522_5523insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000395826.7:c.-21+329_-21+330insC MANE Select ENSP00000379170.2:n.-21+329_-21+330insC
ENST00000264708.7:c.-101+329_-101+330insC ENSP00000264708.3:n.-101+329_-101+330insC
ENST00000380794.5:c.-71+329_-71+330insC ENSP00000370171.1:n.-71+329_-71+330insC
ENST00000395826.6:c.-21+329_-21+330insC ENSP00000379170.2:n.-21+329_-21+330insC
ENST00000405623.5:c.-51+329_-51+330insC ENSP00000384092.1:n.-51+329_-51+330insC
ENST00000449220.1:c.-71+329_-71+330insC ENSP00000387993.1:n.-71+329_-71+330insC
NM_000939.2:c.-21+329_-21+330insC NP_000930.1:n.-21+329_-21+330insC
NM_001035256.1:c.-71+329_-71+330insC NP_001030333.1:n.-71+329_-71+330insC
XM_011532917.1:c.-51+329_-51+330insC XP_011531219.1:n.-51+329_-51+330insC
NM_000939.3:c.-21+329_-21+330insC NP_000930.1:n.-21+329_-21+330insC
NM_001035256.2:c.-71+329_-71+330insC NP_001030333.1:n.-71+329_-71+330insC
NM_001319204.1:c.-101+329_-101+330insC NP_001306133.1:n.-101+329_-101+330insC
NM_001319205.1:c.-51+329_-51+330insC NP_001306134.1:n.-51+329_-51+330insC
NM_000939.4:c.-21+329_-21+330insC MANE Select NP_000930.1:n.-21+329_-21+330insC
NM_001319204.2:c.-101+329_-101+330insC NP_001306133.1:n.-101+329_-101+330insC
NM_001319205.2:c.-51+329_-51+330insC NP_001306134.1:n.-51+329_-51+330insC
NM_001035256.3:c.-71+329_-71+330insC NP_001030333.1:n.-71+329_-71+330insC