Canonical Allele Identifier: CA2617231151
Gene: VWF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031661_6031662del , CM000674.2:g.6031661_6031662del GRCh38
NC_000012.11:g.6140827_6140828del , CM000674.1:g.6140827_6140828del GRCh37
NC_000012.10:g.6011088_6011089del NCBI36
NG_009072.1:g.98009_98010del
NG_009072.2:g.98009_98010del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2686-84_2686-83del MANE Select ENSP00000261405.5:n.2686-84_2686-83del
ENST00000261405.9:c.2686-84_2686-83del ENSP00000261405.5:n.2686-84_2686-83del
ENST00000538635.5:n.421-37728_421-37727del
NM_000552.3:c.2686-84_2686-83del NP_000543.2:n.2686-84_2686-83del
NM_000552.4:c.2686-84_2686-83del NP_000543.2:n.2686-84_2686-83del
NM_000552.5:c.2686-84_2686-83del MANE Select NP_000543.3:n.2686-84_2686-83del