Canonical Allele Identifier: CA2617230451

Gene: VWF

Linked Data

• gnomAD v4: 12-6023893-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023895del , CM000674.2:g.6023895del	GRCh38
NC_000012.11:g.6133061del , CM000674.1:g.6133061del	GRCh37
NC_000012.10:g.6003322del	NCBI36
NG_009072.1:g.105777del
NG_009072.2:g.105777del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-107del MANE Select	ENSP00000261405.5:n.3223-107del
ENST00000261405.9:c.3223-107del	ENSP00000261405.5:n.3223-107del
ENST00000538635.5:n.421-29960del
NM_000552.3:c.3223-107del	NP_000543.2:n.3223-107del
NM_000552.4:c.3223-107del	NP_000543.2:n.3223-107del
NM_000552.5:c.3223-107del MANE Select	NP_000543.3:n.3223-107del