Canonical Allele Identifier: CA915943713

Gene: POMC

Linked Data

• ClinVar Variation Id: 666581
• ClinVar RCV Id: RCV000825007
• dbSNP Id: rs1573250294

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161469dup , CM000664.2:g.25161469dup	GRCh38
NC_000002.11:g.25384338dup , CM000664.1:g.25384338dup	GRCh37
NC_000002.10:g.25237842dup	NCBI36
NG_008997.1:g.12222dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000395826.7:c.416dup MANE Select	ENSP00000379170.2:p.Tyr139Ter
ENST00000264708.7:c.416dup	ENSP00000264708.3:p.Tyr139Ter
ENST00000380794.5:c.416dup	ENSP00000370171.1:p.Tyr139Ter
ENST00000395826.6:c.416dup	ENSP00000379170.2:p.Tyr139Ter
ENST00000405623.5:c.416dup	ENSP00000384092.1:p.Tyr139Ter
ENST00000449220.1:c.416dup	ENSP00000387993.1:p.Tyr139Ter
NM_000939.2:c.416dup	NP_000930.1:p.Tyr139Ter
NM_001035256.1:c.416dup	NP_001030333.1:p.Tyr139Ter
XM_011532917.1:c.416dup	XP_011531219.1:p.Tyr139Ter
NM_000939.3:c.416dup	NP_000930.1:p.Tyr139Ter
NM_001035256.2:c.416dup	NP_001030333.1:p.Tyr139Ter
NM_001319204.1:c.416dup	NP_001306133.1:p.Tyr139Ter
NM_001319205.1:c.416dup	NP_001306134.1:p.Tyr139Ter
NM_000939.4:c.416dup MANE Select	NP_000930.1:p.Tyr139Ter
NM_001319204.2:c.416dup	NP_001306133.1:p.Tyr139Ter
NM_001319205.2:c.416dup	NP_001306134.1:p.Tyr139Ter
NM_001035256.3:c.416dup	NP_001030333.1:p.Tyr139Ter