Canonical Allele Identifier: CA2794406787
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6058118del , CM000674.2:g.6058118del GRCh38
NC_000012.11:g.6167284del , CM000674.1:g.6167284del GRCh37
NC_000012.10:g.6037545del NCBI36
NG_009072.1:g.71554del
NG_009072.2:g.71554del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1534-73del MANE Select ENSP00000261405.5:n.1534-73del
ENST00000261405.9:c.1534-73del ENSP00000261405.5:n.1534-73del
ENST00000538635.5:n.420+52398del
NM_000552.3:c.1534-73del NP_000543.2:n.1534-73del
NM_000552.4:c.1534-73del NP_000543.2:n.1534-73del
NM_000552.5:c.1534-73del MANE Select NP_000543.3:n.1534-73del