Canonical Allele Identifier: CA2617232720

Gene: VWF

Linked Data

• gnomAD v4: 12-6058121-T-TTAATAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058122_6058129dup , CM000674.2:g.6058122_6058129dup	GRCh38
NC_000012.11:g.6167288_6167295dup , CM000674.1:g.6167288_6167295dup	GRCh37
NC_000012.10:g.6037549_6037556dup	NCBI36
NG_009072.1:g.71542_71549dup
NG_009072.2:g.71542_71549dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1534-85_1534-78dup MANE Select	ENSP00000261405.5:n.1534-85_1534-78dup
ENST00000261405.9:c.1534-85_1534-78dup	ENSP00000261405.5:n.1534-85_1534-78dup
ENST00000538635.5:n.420+52386_420+52393dup
NM_000552.3:c.1534-85_1534-78dup	NP_000543.2:n.1534-85_1534-78dup
NM_000552.4:c.1534-85_1534-78dup	NP_000543.2:n.1534-85_1534-78dup
NM_000552.5:c.1534-85_1534-78dup MANE Select	NP_000543.3:n.1534-85_1534-78dup