Canonical Allele Identifier: CA2617232719

Gene: VWF

Linked Data

• gnomAD v4: 12-6058121-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058121_6058122insA , CM000674.2:g.6058121_6058122insA	GRCh38
NC_000012.11:g.6167287_6167288insA , CM000674.1:g.6167287_6167288insA	GRCh37
NC_000012.10:g.6037548_6037549insA	NCBI36
NG_009072.1:g.71549_71550insT
NG_009072.2:g.71549_71550insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1534-78_1534-77insT MANE Select	ENSP00000261405.5:n.1534-78_1534-77insT
ENST00000261405.9:c.1534-78_1534-77insT	ENSP00000261405.5:n.1534-78_1534-77insT
ENST00000538635.5:n.420+52393_420+52394insT
NM_000552.3:c.1534-78_1534-77insT	NP_000543.2:n.1534-78_1534-77insT
NM_000552.4:c.1534-78_1534-77insT	NP_000543.2:n.1534-78_1534-77insT
NM_000552.5:c.1534-78_1534-77insT MANE Select	NP_000543.3:n.1534-78_1534-77insT