Canonical Allele Identifier: CA1239231224
Gene: POMC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25164239G= , CM000664.2:g.25164239G= GRCh38
NC_000002.11:g.25387108G= , CM000664.1:g.25387108G= GRCh37
NC_000002.10:g.25240612G= NCBI36
NG_008997.1:g.9452C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.132+402C= MANE Select ENSP00000379170.2:n.132+402C=
ENST00000264708.7:c.132+402C= ENSP00000264708.3:n.132+402C=
ENST00000380794.5:c.132+402C= ENSP00000370171.1:n.132+402C=
ENST00000395826.6:c.132+402C= ENSP00000379170.2:n.132+402C=
ENST00000405623.5:c.132+402C= ENSP00000384092.1:n.132+402C=
ENST00000449220.1:c.132+402C= ENSP00000387993.1:n.132+402C=
NM_000939.2:c.132+402C= NP_000930.1:n.132+402C=
NM_001035256.1:c.132+402C= NP_001030333.1:n.132+402C=
XM_011532917.1:c.132+402C= XP_011531219.1:n.132+402C=
NM_000939.3:c.132+402C= NP_000930.1:n.132+402C=
NM_001035256.2:c.132+402C= NP_001030333.1:n.132+402C=
NM_001319204.1:c.132+402C= NP_001306133.1:n.132+402C=
NM_001319205.1:c.132+402C= NP_001306134.1:n.132+402C=
NM_000939.4:c.132+402C= MANE Select NP_000930.1:n.132+402C=
NM_001319204.2:c.132+402C= NP_001306133.1:n.132+402C=
NM_001319205.2:c.132+402C= NP_001306134.1:n.132+402C=
NM_001035256.3:c.132+402C= NP_001030333.1:n.132+402C=