Canonical Allele Identifier: CA139599364

Gene: HCRTR2

Linked Data

• dbSNP Id: rs922918834
• gnomAD v3: 6-55180289-T-TCCA
• gnomAD v4: 6-55180289-T-TCCA
• MyVariant Identifiers: chr6:g.55045087_55045088insCCA (hg19) ; chr6:g.55180289_55180290insCCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55180290_55180292dup , CM000668.2:g.55180290_55180292dup	GRCh38
NC_000006.11:g.55045088_55045090dup , CM000668.1:g.55045088_55045090dup	GRCh37
NC_000006.10:g.55153047_55153049dup	NCBI36
NG_012447.1:g.11018_11020dup
NG_012447.2:g.78831_78833dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.223+5480_223+5482dup MANE Select	ENSP00000359899.3:n.223+5480_223+5482dup
ENST00000370862.3:c.223+5480_223+5482dup	ENSP00000359899.3:n.223+5480_223+5482dup
ENST00000615358.4:c.223+5480_223+5482dup	ENSP00000477548.1:n.223+5480_223+5482dup
NM_001526.3:c.223+5480_223+5482dup	NP_001517.2:n.223+5480_223+5482dup
NM_001526.4:c.223+5480_223+5482dup	NP_001517.2:n.223+5480_223+5482dup
XM_017010798.1:c.223+5480_223+5482dup	XP_016866287.1:n.223+5480_223+5482dup
NM_001384272.1:c.223+5480_223+5482dup MANE Select	NP_001371201.1:n.223+5480_223+5482dup
NM_001526.5:c.223+5480_223+5482dup	NP_001517.2:n.223+5480_223+5482dup