Canonical Allele Identifier: CA2617232726

Gene: VWF

Linked Data

• gnomAD v4: 12-6058124-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058124_6058125insC , CM000674.2:g.6058124_6058125insC	GRCh38
NC_000012.11:g.6167290_6167291insC , CM000674.1:g.6167290_6167291insC	GRCh37
NC_000012.10:g.6037551_6037552insC	NCBI36
NG_009072.1:g.71546_71547insG
NG_009072.2:g.71546_71547insG

Transcript Alleles

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