Canonical Allele Identifier: CA531358435
Gene: POMC HGNC NCBI

Linked Data

dbSNP Id: rs1252693585

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25161616dup , CM000664.2:g.25161616dup GRCh38
NC_000002.11:g.25384485dup , CM000664.1:g.25384485dup GRCh37
NC_000002.10:g.25237989dup NCBI36
NG_008997.1:g.12075dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395826.7:c.269dup MANE Select ENSP00000379170.2:p.Asn91GlnfsTer28
ENST00000264708.7:c.269dup ENSP00000264708.3:p.Asn91GlnfsTer28
ENST00000380794.5:c.269dup ENSP00000370171.1:p.Asn91GlnfsTer28
ENST00000395826.6:c.269dup ENSP00000379170.2:p.Asn91GlnfsTer28
ENST00000405623.5:c.269dup ENSP00000384092.1:p.Asn91GlnfsTer28
ENST00000449220.1:c.269dup ENSP00000387993.1:p.Asn91GlnfsTer28
NM_000939.2:c.269dup NP_000930.1:p.Asn91GlnfsTer28
NM_001035256.1:c.269dup NP_001030333.1:p.Asn91GlnfsTer28
XM_011532917.1:c.269dup XP_011531219.1:p.Asn91GlnfsTer28
NM_000939.3:c.269dup NP_000930.1:p.Asn91GlnfsTer28
NM_001035256.2:c.269dup NP_001030333.1:p.Asn91GlnfsTer28
NM_001319204.1:c.269dup NP_001306133.1:p.Asn91GlnfsTer28
NM_001319205.1:c.269dup NP_001306134.1:p.Asn91GlnfsTer28
NM_000939.4:c.269dup MANE Select NP_000930.1:p.Asn91GlnfsTer28
NM_001319204.2:c.269dup NP_001306133.1:p.Asn91GlnfsTer28
NM_001319205.2:c.269dup NP_001306134.1:p.Asn91GlnfsTer28
NM_001035256.3:c.269dup NP_001030333.1:p.Asn91GlnfsTer28