Canonical Allele Identifier: CA2576693514
Gene: POMC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25161587_25161588insACCGCTGCT , CM000664.2:g.25161587_25161588insACCGCTGCT GRCh38
NC_000002.11:g.25384456_25384457insACCGCTGCT , CM000664.1:g.25384456_25384457insACCGCTGCT GRCh37
NC_000002.10:g.25237960_25237961insACCGCTGCT NCBI36
NG_008997.1:g.12103_12104insAGCAGCGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.297_298insAGCAGCGGT MANE Select ENSP00000379170.2:p.Gly99_Ala100insSerSerGly
ENST00000264708.7:c.297_298insAGCAGCGGT ENSP00000264708.3:p.Gly99_Ala100insSerSerGly
ENST00000380794.5:c.297_298insAGCAGCGGT ENSP00000370171.1:p.Gly99_Ala100insSerSerGly
ENST00000395826.6:c.297_298insAGCAGCGGT ENSP00000379170.2:p.Gly99_Ala100insSerSerGly
ENST00000405623.5:c.297_298insAGCAGCGGT ENSP00000384092.1:p.Gly99_Ala100insSerSerGly
ENST00000449220.1:c.297_298insAGCAGCGGT ENSP00000387993.1:p.Gly99_Ala100insSerSerGly
NM_000939.2:c.297_298insAGCAGCGGT NP_000930.1:p.Gly99_Ala100insSerSerGly
NM_001035256.1:c.297_298insAGCAGCGGT NP_001030333.1:p.Gly99_Ala100insSerSerGly
XM_011532917.1:c.297_298insAGCAGCGGT XP_011531219.1:p.Gly99_Ala100insSerSerGly
NM_000939.3:c.297_298insAGCAGCGGT NP_000930.1:p.Gly99_Ala100insSerSerGly
NM_001035256.2:c.297_298insAGCAGCGGT NP_001030333.1:p.Gly99_Ala100insSerSerGly
NM_001319204.1:c.297_298insAGCAGCGGT NP_001306133.1:p.Gly99_Ala100insSerSerGly
NM_001319205.1:c.297_298insAGCAGCGGT NP_001306134.1:p.Gly99_Ala100insSerSerGly
NM_000939.4:c.297_298insAGCAGCGGT MANE Select NP_000930.1:p.Gly99_Ala100insSerSerGly
NM_001319204.2:c.297_298insAGCAGCGGT NP_001306133.1:p.Gly99_Ala100insSerSerGly
NM_001319205.2:c.297_298insAGCAGCGGT NP_001306134.1:p.Gly99_Ala100insSerSerGly
NM_001035256.3:c.297_298insAGCAGCGGT NP_001030333.1:p.Gly99_Ala100insSerSerGly