Canonical Allele Identifier: CA2617231148

Gene: VWF

Linked Data

• gnomAD v4: 12-6031654-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031655dup , CM000674.2:g.6031655dup	GRCh38
NC_000012.11:g.6140821dup , CM000674.1:g.6140821dup	GRCh37
NC_000012.10:g.6011082dup	NCBI36
NG_009072.1:g.98016dup
NG_009072.2:g.98016dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2686-77dup MANE Select	ENSP00000261405.5:n.2686-77dup
ENST00000261405.9:c.2686-77dup	ENSP00000261405.5:n.2686-77dup
ENST00000538635.5:n.421-37721dup
NM_000552.3:c.2686-77dup	NP_000543.2:n.2686-77dup
NM_000552.4:c.2686-77dup	NP_000543.2:n.2686-77dup
NM_000552.5:c.2686-77dup MANE Select	NP_000543.3:n.2686-77dup