Canonical Allele Identifier: CA2617230455
Gene: VWF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023896_6023897insTTG , CM000674.2:g.6023896_6023897insTTG GRCh38
NC_000012.11:g.6133062_6133063insTTG , CM000674.1:g.6133062_6133063insTTG GRCh37
NC_000012.10:g.6003323_6003324insTTG NCBI36
NG_009072.1:g.105774_105775insCAA
NG_009072.2:g.105774_105775insCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3223-110_3223-109insCAA MANE Select ENSP00000261405.5:n.3223-110_3223-109insCAA
ENST00000261405.9:c.3223-110_3223-109insCAA ENSP00000261405.5:n.3223-110_3223-109insCAA
ENST00000538635.5:n.421-29963_421-29962insCAA
NM_000552.3:c.3223-110_3223-109insCAA NP_000543.2:n.3223-110_3223-109insCAA
NM_000552.4:c.3223-110_3223-109insCAA NP_000543.2:n.3223-110_3223-109insCAA
NM_000552.5:c.3223-110_3223-109insCAA MANE Select NP_000543.3:n.3223-110_3223-109insCAA