Canonical Allele Identifier: CA2497154672

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1767075483

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55276297_55276304del , CM000668.2:g.55276297_55276304del	GRCh38
NC_000006.11:g.55141095_55141102del , CM000668.1:g.55141095_55141102del	GRCh37
NC_000006.10:g.55249054_55249061del	NCBI36
NG_012447.1:g.107025_107032del
NG_012447.2:g.174838_174845del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.763-1083_763-1076del MANE Select	ENSP00000359899.3:n.763-1083_763-1076del
ENST00000370862.3:c.763-1083_763-1076del	ENSP00000359899.3:n.763-1083_763-1076del
ENST00000615358.4:c.763-1083_763-1076del	ENSP00000477548.1:n.763-1083_763-1076del
NM_001526.3:c.763-1083_763-1076del	NP_001517.2:n.763-1083_763-1076del
XM_011514542.1:c.568-1083_568-1076del	XP_011512844.1:n.568-1083_568-1076del
NM_001526.4:c.763-1083_763-1076del	NP_001517.2:n.763-1083_763-1076del
XM_017010798.1:c.763-1083_763-1076del	XP_016866287.1:n.763-1083_763-1076del
NM_001384272.1:c.763-1083_763-1076del MANE Select	NP_001371201.1:n.763-1083_763-1076del
NM_001526.5:c.763-1083_763-1076del	NP_001517.2:n.763-1083_763-1076del