Canonical Allele Identifier: CA2497154673
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1767075943

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55276345_55276349del , CM000668.2:g.55276345_55276349del GRCh38
NC_000006.11:g.55141143_55141147del , CM000668.1:g.55141143_55141147del GRCh37
NC_000006.10:g.55249102_55249106del NCBI36
NG_012447.1:g.107073_107077del
NG_012447.2:g.174886_174890del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370862.4:c.763-1035_763-1031del MANE Select ENSP00000359899.3:n.763-1035_763-1031del
ENST00000370862.3:c.763-1035_763-1031del ENSP00000359899.3:n.763-1035_763-1031del
ENST00000615358.4:c.763-1035_763-1031del ENSP00000477548.1:n.763-1035_763-1031del
NM_001526.3:c.763-1035_763-1031del NP_001517.2:n.763-1035_763-1031del
XM_011514542.1:c.568-1035_568-1031del XP_011512844.1:n.568-1035_568-1031del
NM_001526.4:c.763-1035_763-1031del NP_001517.2:n.763-1035_763-1031del
XM_017010798.1:c.763-1035_763-1031del XP_016866287.1:n.763-1035_763-1031del
NM_001384272.1:c.763-1035_763-1031del MANE Select NP_001371201.1:n.763-1035_763-1031del
NM_001526.5:c.763-1035_763-1031del NP_001517.2:n.763-1035_763-1031del