Canonical Allele Identifier: CA2740746023

Gene: HCRTR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269320_55269321del , CM000668.2:g.55269320_55269321del	GRCh38
NC_000006.11:g.55134118_55134119del , CM000668.1:g.55134118_55134119del	GRCh37
NC_000006.10:g.55242077_55242078del	NCBI36
NG_012447.1:g.100048_100049del
NG_012447.2:g.167861_167862del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.762+5498_762+5499del MANE Select	ENSP00000359899.3:n.762+5498_762+5499del
ENST00000370862.3:c.762+5498_762+5499del	ENSP00000359899.3:n.762+5498_762+5499del
ENST00000615358.4:c.762+5498_762+5499del	ENSP00000477548.1:n.762+5498_762+5499del
NM_001526.3:c.762+5498_762+5499del	NP_001517.2:n.762+5498_762+5499del
XM_011514542.1:c.567+5498_567+5499del	XP_011512844.1:n.567+5498_567+5499del
NM_001526.4:c.762+5498_762+5499del	NP_001517.2:n.762+5498_762+5499del
XM_017010798.1:c.762+5498_762+5499del	XP_016866287.1:n.762+5498_762+5499del
NM_001384272.1:c.762+5498_762+5499del MANE Select	NP_001371201.1:n.762+5498_762+5499del
NM_001526.5:c.762+5498_762+5499del	NP_001517.2:n.762+5498_762+5499del