Canonical Allele Identifier: CA2575053927
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023552del , CM000674.2:g.6023552del GRCh38
NC_000012.11:g.6132718del , CM000674.1:g.6132718del GRCh37
NC_000012.10:g.6002979del NCBI36
NG_009072.1:g.106123del
NG_009072.2:g.106123del

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3379+83del MANE Select ENSP00000261405.5:n.3379+83del
ENST00000261405.9:c.3379+83del ENSP00000261405.5:n.3379+83del
ENST00000538635.5:n.421-29614del
NM_000552.3:c.3379+83del NP_000543.2:n.3379+83del
NM_000552.4:c.3379+83del NP_000543.2:n.3379+83del
NM_000552.5:c.3379+83del MANE Select NP_000543.3:n.3379+83del