Canonical Allele Identifier: CA567639513
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1478494754

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55248631_55248634del , CM000668.2:g.55248631_55248634del GRCh38
NC_000006.11:g.55113429_55113432del , CM000668.1:g.55113429_55113432del GRCh37
NC_000006.10:g.55221388_55221391del NCBI36
NG_012447.1:g.79359_79362del
NG_012447.2:g.147172_147175del

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.224-8_224-5del MANE Select ENSP00000359899.3:n.224-8_224-5del
ENST00000370862.3:c.224-8_224-5del ENSP00000359899.3:n.224-8_224-5del
ENST00000615358.4:c.224-8_224-5del ENSP00000477548.1:n.224-8_224-5del
NM_001526.3:c.224-8_224-5del NP_001517.2:n.224-8_224-5del
XM_011514542.1:c.29-8_29-5del XP_011512844.1:n.29-8_29-5del
NM_001526.4:c.224-8_224-5del NP_001517.2:n.224-8_224-5del
XM_017010798.1:c.224-8_224-5del XP_016866287.1:n.224-8_224-5del
NM_001384272.1:c.224-8_224-5del MANE Select NP_001371201.1:n.224-8_224-5del
NM_001526.5:c.224-8_224-5del NP_001517.2:n.224-8_224-5del