Canonical Allele Identifier: CA1239227081

Gene: POMC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161220C= , CM000664.2:g.25161220C=	GRCh38
NC_000002.11:g.25384089C= , CM000664.1:g.25384089C=	GRCh37
NC_000002.10:g.25237593C=	NCBI36
NG_008997.1:g.12471G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395826.7:c.665G= MANE Select	ENSP00000379170.2:p.Arg222=
ENST00000264708.7:c.665G=	ENSP00000264708.3:p.Arg222=
ENST00000380794.5:c.665G=	ENSP00000370171.1:p.Arg222=
ENST00000395826.6:c.665G=	ENSP00000379170.2:p.Arg222=
ENST00000405623.5:c.665G=	ENSP00000384092.1:p.Arg222=
ENST00000449220.1:c.665G=	ENSP00000387993.1:p.Arg222=
NM_000939.2:c.665G=	NP_000930.1:p.Arg222=
NM_001035256.1:c.665G=	NP_001030333.1:p.Arg222=
XM_011532917.1:c.665G=	XP_011531219.1:p.Arg222=
NM_000939.3:c.665G=	NP_000930.1:p.Arg222=
NM_001035256.2:c.665G=	NP_001030333.1:p.Arg222=
NM_001319204.1:c.665G=	NP_001306133.1:p.Arg222=
NM_001319205.1:c.665G=	NP_001306134.1:p.Arg222=
NM_000939.4:c.665G= MANE Select	NP_000930.1:p.Arg222=
NM_001319204.2:c.665G=	NP_001306133.1:p.Arg222=
NM_001319205.2:c.665G=	NP_001306134.1:p.Arg222=
NM_001035256.3:c.665G=	NP_001030333.1:p.Arg222=