Canonical Allele Identifier: CA2617232725

Gene: VWF

Linked Data

• gnomAD v4: 12-6058123-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058125_6058126del , CM000674.2:g.6058125_6058126del	GRCh38
NC_000012.11:g.6167291_6167292del , CM000674.1:g.6167291_6167292del	GRCh37
NC_000012.10:g.6037552_6037553del	NCBI36
NG_009072.1:g.71546_71547del
NG_009072.2:g.71546_71547del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1534-81_1534-80del MANE Select	ENSP00000261405.5:n.1534-81_1534-80del
ENST00000261405.9:c.1534-81_1534-80del	ENSP00000261405.5:n.1534-81_1534-80del
ENST00000538635.5:n.420+52390_420+52391del
NM_000552.3:c.1534-81_1534-80del	NP_000543.2:n.1534-81_1534-80del
NM_000552.4:c.1534-81_1534-80del	NP_000543.2:n.1534-81_1534-80del
NM_000552.5:c.1534-81_1534-80del MANE Select	NP_000543.3:n.1534-81_1534-80del