Canonical Allele Identifier: CA139610166

Gene: HCRTR2

Linked Data

• dbSNP Id: rs995784549
• gnomAD v2: 6-55134272-C-CA
• gnomAD v3: 6-55269474-C-CA
• gnomAD v4: 6-55269474-C-CA
• MyVariant Identifiers: chr6:g.55134273_55134274insA (hg19) ; chr6:g.55134272_55134273insA (hg19) ; chr6:g.55269475_55269476insA (hg38) ; chr6:g.55269474_55269475insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269481dup , CM000668.2:g.55269481dup	GRCh38
NC_000006.11:g.55134279dup , CM000668.1:g.55134279dup	GRCh37
NC_000006.10:g.55242238dup	NCBI36
NG_012447.1:g.100209dup
NG_012447.2:g.168022dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.762+5659dup MANE Select	ENSP00000359899.3:n.762+5659dup
ENST00000370862.3:c.762+5659dup	ENSP00000359899.3:n.762+5659dup
ENST00000615358.4:c.762+5659dup	ENSP00000477548.1:n.762+5659dup
NM_001526.3:c.762+5659dup	NP_001517.2:n.762+5659dup
XM_011514542.1:c.567+5659dup	XP_011512844.1:n.567+5659dup
NM_001526.4:c.762+5659dup	NP_001517.2:n.762+5659dup
XM_017010798.1:c.762+5659dup	XP_016866287.1:n.762+5659dup
NM_001384272.1:c.762+5659dup MANE Select	NP_001371201.1:n.762+5659dup
NM_001526.5:c.762+5659dup	NP_001517.2:n.762+5659dup