Canonical Allele Identifier: CA1239227402
Gene: POMC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25161364A= , CM000664.2:g.25161364A= GRCh38
NC_000002.11:g.25384233A= , CM000664.1:g.25384233A= GRCh37
NC_000002.10:g.25237737A= NCBI36
NG_008997.1:g.12327T=

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.521T= MANE Select ENSP00000379170.2:p.Leu174=
ENST00000264708.7:c.521T= ENSP00000264708.3:p.Leu174=
ENST00000380794.5:c.521T= ENSP00000370171.1:p.Leu174=
ENST00000395826.6:c.521T= ENSP00000379170.2:p.Leu174=
ENST00000405623.5:c.521T= ENSP00000384092.1:p.Leu174=
ENST00000449220.1:c.521T= ENSP00000387993.1:p.Leu174=
NM_000939.2:c.521T= NP_000930.1:p.Leu174=
NM_001035256.1:c.521T= NP_001030333.1:p.Leu174=
XM_011532917.1:c.521T= XP_011531219.1:p.Leu174=
NM_000939.3:c.521T= NP_000930.1:p.Leu174=
NM_001035256.2:c.521T= NP_001030333.1:p.Leu174=
NM_001319204.1:c.521T= NP_001306133.1:p.Leu174=
NM_001319205.1:c.521T= NP_001306134.1:p.Leu174=
NM_000939.4:c.521T= MANE Select NP_000930.1:p.Leu174=
NM_001319204.2:c.521T= NP_001306133.1:p.Leu174=
NM_001319205.2:c.521T= NP_001306134.1:p.Leu174=
NM_001035256.3:c.521T= NP_001030333.1:p.Leu174=