Canonical Allele Identifier: CA826027466

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1488959797
• gnomAD v3: 6-55269304-ATT-A
• gnomAD v4: 6-55269304-ATT-A
• MyVariant Identifiers: chr6:g.55134103_55134104del (hg19) ; chr6:g.55269305_55269306del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269307_55269308del , CM000668.2:g.55269307_55269308del	GRCh38
NC_000006.11:g.55134105_55134106del , CM000668.1:g.55134105_55134106del	GRCh37
NC_000006.10:g.55242064_55242065del	NCBI36
NG_012447.1:g.100035_100036del
NG_012447.2:g.167848_167849del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370862.4:c.762+5485_762+5486del MANE Select	ENSP00000359899.3:n.762+5485_762+5486del
ENST00000370862.3:c.762+5485_762+5486del	ENSP00000359899.3:n.762+5485_762+5486del
ENST00000615358.4:c.762+5485_762+5486del	ENSP00000477548.1:n.762+5485_762+5486del
NM_001526.3:c.762+5485_762+5486del	NP_001517.2:n.762+5485_762+5486del
XM_011514542.1:c.567+5485_567+5486del	XP_011512844.1:n.567+5485_567+5486del
NM_001526.4:c.762+5485_762+5486del	NP_001517.2:n.762+5485_762+5486del
XM_017010798.1:c.762+5485_762+5486del	XP_016866287.1:n.762+5485_762+5486del
NM_001384272.1:c.762+5485_762+5486del MANE Select	NP_001371201.1:n.762+5485_762+5486del
NM_001526.5:c.762+5485_762+5486del	NP_001517.2:n.762+5485_762+5486del