Canonical Allele Identifier: CA2502614831

Gene: HCRTR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269404_55269411del , CM000668.2:g.55269404_55269411del	GRCh38
NC_000006.11:g.55134202_55134209del , CM000668.1:g.55134202_55134209del	GRCh37
NC_000006.10:g.55242161_55242168del	NCBI36
NG_012447.1:g.100132_100139del
NG_012447.2:g.167945_167952del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.762+5582_762+5589del MANE Select	ENSP00000359899.3:n.762+5582_762+5589del
ENST00000370862.3:c.762+5582_762+5589del	ENSP00000359899.3:n.762+5582_762+5589del
ENST00000615358.4:c.762+5582_762+5589del	ENSP00000477548.1:n.762+5582_762+5589del
NM_001526.3:c.762+5582_762+5589del	NP_001517.2:n.762+5582_762+5589del
XM_011514542.1:c.567+5582_567+5589del	XP_011512844.1:n.567+5582_567+5589del
NM_001526.4:c.762+5582_762+5589del	NP_001517.2:n.762+5582_762+5589del
XM_017010798.1:c.762+5582_762+5589del	XP_016866287.1:n.762+5582_762+5589del
NM_001384272.1:c.762+5582_762+5589del MANE Select	NP_001371201.1:n.762+5582_762+5589del
NM_001526.5:c.762+5582_762+5589del	NP_001517.2:n.762+5582_762+5589del