Canonical Allele Identifier: CA567488246
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1298180542

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55276349_55276351del , CM000668.2:g.55276349_55276351del GRCh38
NC_000006.11:g.55141147_55141149del , CM000668.1:g.55141147_55141149del GRCh37
NC_000006.10:g.55249106_55249108del NCBI36
NG_012447.1:g.107077_107079del
NG_012447.2:g.174890_174892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370862.4:c.763-1031_763-1029del MANE Select ENSP00000359899.3:n.763-1031_763-1029del
ENST00000370862.3:c.763-1031_763-1029del ENSP00000359899.3:n.763-1031_763-1029del
ENST00000615358.4:c.763-1031_763-1029del ENSP00000477548.1:n.763-1031_763-1029del
NM_001526.3:c.763-1031_763-1029del NP_001517.2:n.763-1031_763-1029del
XM_011514542.1:c.568-1031_568-1029del XP_011512844.1:n.568-1031_568-1029del
NM_001526.4:c.763-1031_763-1029del NP_001517.2:n.763-1031_763-1029del
XM_017010798.1:c.763-1031_763-1029del XP_016866287.1:n.763-1031_763-1029del
NM_001384272.1:c.763-1031_763-1029del MANE Select NP_001371201.1:n.763-1031_763-1029del
NM_001526.5:c.763-1031_763-1029del NP_001517.2:n.763-1031_763-1029del