Canonical Allele Identifier: CA2497154578

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1766929126

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269431_55269433del , CM000668.2:g.55269431_55269433del	GRCh38
NC_000006.11:g.55134229_55134231del , CM000668.1:g.55134229_55134231del	GRCh37
NC_000006.10:g.55242188_55242190del	NCBI36
NG_012447.1:g.100159_100161del
NG_012447.2:g.167972_167974del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370862.4:c.762+5609_762+5611del MANE Select	ENSP00000359899.3:n.762+5609_762+5611del
ENST00000370862.3:c.762+5609_762+5611del	ENSP00000359899.3:n.762+5609_762+5611del
ENST00000615358.4:c.762+5609_762+5611del	ENSP00000477548.1:n.762+5609_762+5611del
NM_001526.3:c.762+5609_762+5611del	NP_001517.2:n.762+5609_762+5611del
XM_011514542.1:c.567+5609_567+5611del	XP_011512844.1:n.567+5609_567+5611del
NM_001526.4:c.762+5609_762+5611del	NP_001517.2:n.762+5609_762+5611del
XM_017010798.1:c.762+5609_762+5611del	XP_016866287.1:n.762+5609_762+5611del
NM_001384272.1:c.762+5609_762+5611del MANE Select	NP_001371201.1:n.762+5609_762+5611del
NM_001526.5:c.762+5609_762+5611del	NP_001517.2:n.762+5609_762+5611del