Canonical Allele Identifier: CA1239226617

Gene: POMC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25160982C= , CM000664.2:g.25160982C=	GRCh38
NC_000002.11:g.25383851C= , CM000664.1:g.25383851C=	GRCh37
NC_000002.10:g.25237355C=	NCBI36
NG_008997.1:g.12709G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395826.7:c.*99G= MANE Select	ENSP00000379170.2:n.*99G=
ENST00000380794.5:c.*99G=	ENSP00000370171.1:n.*99G=
ENST00000405623.5:c.*99G=	ENSP00000384092.1:n.*99G=
NM_000939.2:c.*99G=	NP_000930.1:n.*99G=
NM_001035256.1:c.*99G=	NP_001030333.1:n.*99G=
XM_011532917.1:c.*99G=	XP_011531219.1:n.*99G=
NM_000939.3:c.*99G=	NP_000930.1:n.*99G=
NM_001035256.2:c.*99G=	NP_001030333.1:n.*99G=
NM_001319204.1:c.*99G=	NP_001306133.1:n.*99G=
NM_001319205.1:c.*99G=	NP_001306134.1:n.*99G=
NM_000939.4:c.*99G= MANE Select	NP_000930.1:n.*99G=
NM_001319204.2:c.*99G=	NP_001306133.1:n.*99G=
NM_001319205.2:c.*99G=	NP_001306134.1:n.*99G=
NM_001035256.3:c.*99G=	NP_001030333.1:n.*99G=