Canonical Allele Identifier: CA1239233114
Gene: POMC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25167009G= , CM000664.2:g.25167009G= GRCh38
NC_000002.11:g.25389878G= , CM000664.1:g.25389878G= GRCh37
NC_000002.10:g.25243382G= NCBI36
NG_008997.1:g.6682C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395826.7:c.-21+1489C= MANE Select ENSP00000379170.2:n.-21+1489C=
ENST00000264708.7:c.-100-1324C= ENSP00000264708.3:n.-100-1324C=
ENST00000380794.5:c.-70-1324C= ENSP00000370171.1:n.-70-1324C=
ENST00000395826.6:c.-21+1489C= ENSP00000379170.2:n.-21+1489C=
ENST00000405623.5:c.-51+1489C= ENSP00000384092.1:n.-51+1489C=
ENST00000449220.1:c.-70-1324C= ENSP00000387993.1:n.-70-1324C=
NM_000939.2:c.-21+1489C= NP_000930.1:n.-21+1489C=
NM_001035256.1:c.-70-1324C= NP_001030333.1:n.-70-1324C=
XM_011532917.1:c.-51+1489C= XP_011531219.1:n.-51+1489C=
NM_000939.3:c.-21+1489C= NP_000930.1:n.-21+1489C=
NM_001035256.2:c.-70-1324C= NP_001030333.1:n.-70-1324C=
NM_001319204.1:c.-100-1324C= NP_001306133.1:n.-100-1324C=
NM_001319205.1:c.-51+1489C= NP_001306134.1:n.-51+1489C=
NM_000939.4:c.-21+1489C= MANE Select NP_000930.1:n.-21+1489C=
NM_001319204.2:c.-100-1324C= NP_001306133.1:n.-100-1324C=
NM_001319205.2:c.-51+1489C= NP_001306134.1:n.-51+1489C=
NM_001035256.3:c.-70-1324C= NP_001030333.1:n.-70-1324C=