Canonical Allele Identifier: CA567486692

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1183275870
• gnomAD v2: 6-55134075-AACAAG-A
• gnomAD v3: 6-55269277-AACAAG-A
• gnomAD v4: 6-55269277-AACAAG-A
• MyVariant Identifiers: chr6:g.55134076_55134080del (hg19) ; chr6:g.55269278_55269282del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269283_55269287del , CM000668.2:g.55269283_55269287del	GRCh38
NC_000006.11:g.55134081_55134085del , CM000668.1:g.55134081_55134085del	GRCh37
NC_000006.10:g.55242040_55242044del	NCBI36
NG_012447.1:g.100011_100015del
NG_012447.2:g.167824_167828del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.762+5461_762+5465del MANE Select	ENSP00000359899.3:n.762+5461_762+5465del
ENST00000370862.3:c.762+5461_762+5465del	ENSP00000359899.3:n.762+5461_762+5465del
ENST00000615358.4:c.762+5461_762+5465del	ENSP00000477548.1:n.762+5461_762+5465del
NM_001526.3:c.762+5461_762+5465del	NP_001517.2:n.762+5461_762+5465del
XM_011514542.1:c.567+5461_567+5465del	XP_011512844.1:n.567+5461_567+5465del
NM_001526.4:c.762+5461_762+5465del	NP_001517.2:n.762+5461_762+5465del
XM_017010798.1:c.762+5461_762+5465del	XP_016866287.1:n.762+5461_762+5465del
NM_001384272.1:c.762+5461_762+5465del MANE Select	NP_001371201.1:n.762+5461_762+5465del
NM_001526.5:c.762+5461_762+5465del	NP_001517.2:n.762+5461_762+5465del