Canonical Allele Identifier: CA1028505497

Gene: POMC

Linked Data

• gnomAD v3: 2-25161619-C-CTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCT
• gnomAD v4: 2-25161619-C-CTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161619_25161620insTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCT , CM000664.2:g.25161619_25161620insTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCT	GRCh38
NC_000002.11:g.25384488_25384489insTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCT , CM000664.1:g.25384488_25384489insTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCT	GRCh37
NC_000002.10:g.25237992_25237993insTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCT	NCBI36
NG_008997.1:g.12071_12072insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395826.7:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA MANE Select	ENSP00000379170.2:p.Arg89GlnfsTer45
ENST00000264708.7:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	ENSP00000264708.3:p.Arg89GlnfsTer45
ENST00000380794.5:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	ENSP00000370171.1:p.Arg89GlnfsTer45
ENST00000395826.6:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	ENSP00000379170.2:p.Arg89GlnfsTer45
ENST00000405623.5:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	ENSP00000384092.1:p.Arg89GlnfsTer45
ENST00000449220.1:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	ENSP00000387993.1:p.Arg89GlnfsTer45
NM_000939.2:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_000930.1:p.Arg89GlnfsTer45
NM_001035256.1:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_001030333.1:p.Arg89GlnfsTer45
XM_011532917.1:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	XP_011531219.1:p.Arg89GlnfsTer45
NM_000939.3:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_000930.1:p.Arg89GlnfsTer45
NM_001035256.2:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_001030333.1:p.Arg89GlnfsTer45
NM_001319204.1:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_001306133.1:p.Arg89GlnfsTer45
NM_001319205.1:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_001306134.1:p.Arg89GlnfsTer45
NM_000939.4:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA MANE Select	NP_000930.1:p.Arg89GlnfsTer45
NM_001319204.2:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_001306133.1:p.Arg89GlnfsTer45
NM_001319205.2:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_001306134.1:p.Arg89GlnfsTer45
NM_001035256.3:c.265_266insAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCA	NP_001030333.1:p.Arg89GlnfsTer45