Canonical Allele Identifier: CA1028505538
Gene: POMC HGNC NCBI

Linked Data

dbSNP Id: rs1323246915

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25161622_25161623insTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTG , CM000664.2:g.25161622_25161623insTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTG GRCh38
NC_000002.11:g.25384491_25384492insTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTG , CM000664.1:g.25384491_25384492insTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTG GRCh37
NC_000002.10:g.25237995_25237996insTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTGCCGCTGCTG NCBI36
NG_008997.1:g.12068_12069insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA MANE Select ENSP00000379170.2:p.Gly88AlafsTer?
ENST00000264708.7:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA ENSP00000264708.3:p.Gly88AlafsTer?
ENST00000380794.5:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA ENSP00000370171.1:p.Gly88AlafsTer?
ENST00000395826.6:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA ENSP00000379170.2:p.Gly88AlafsTer?
ENST00000405623.5:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA ENSP00000384092.1:p.Gly88AlafsTer?
ENST00000449220.1:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA ENSP00000387993.1:p.Gly88AlafsTer?
NM_000939.2:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_000930.1:p.Gly88AlafsTer?
NM_001035256.1:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_001030333.1:p.Gly88AlafsTer?
XM_011532917.1:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA XP_011531219.1:p.Gly88AlafsTer?
NM_000939.3:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_000930.1:p.Gly88AlafsTer?
NM_001035256.2:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_001030333.1:p.Gly88AlafsTer?
NM_001319204.1:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_001306133.1:p.Gly88AlafsTer?
NM_001319205.1:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_001306134.1:p.Gly88AlafsTer?
NM_000939.4:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA MANE Select NP_000930.1:p.Gly88AlafsTer?
NM_001319204.2:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_001306133.1:p.Gly88AlafsTer?
NM_001319205.2:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_001306134.1:p.Gly88AlafsTer?
NM_001035256.3:c.262_263insCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCAGCAGCGGCA NP_001030333.1:p.Gly88AlafsTer?