Canonical Allele Identifier: CA2497153655

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1765109032

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55180273_55180274del , CM000668.2:g.55180273_55180274del	GRCh38
NC_000006.11:g.55045071_55045072del , CM000668.1:g.55045071_55045072del	GRCh37
NC_000006.10:g.55153030_55153031del	NCBI36
NG_012447.1:g.11001_11002del
NG_012447.2:g.78814_78815del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.223+5463_223+5464del MANE Select	ENSP00000359899.3:n.223+5463_223+5464del
ENST00000370862.3:c.223+5463_223+5464del	ENSP00000359899.3:n.223+5463_223+5464del
ENST00000615358.4:c.223+5463_223+5464del	ENSP00000477548.1:n.223+5463_223+5464del
NM_001526.3:c.223+5463_223+5464del	NP_001517.2:n.223+5463_223+5464del
NM_001526.4:c.223+5463_223+5464del	NP_001517.2:n.223+5463_223+5464del
XM_017010798.1:c.223+5463_223+5464del	XP_016866287.1:n.223+5463_223+5464del
NM_001384272.1:c.223+5463_223+5464del MANE Select	NP_001371201.1:n.223+5463_223+5464del
NM_001526.5:c.223+5463_223+5464del	NP_001517.2:n.223+5463_223+5464del