Canonical Allele Identifier: CA2013872593
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018609_6018610delinsCA , CM000674.2:g.6018609_6018610delinsCA GRCh38
NC_000012.11:g.6127775_6127776delinsCA , CM000674.1:g.6127775_6127776delinsCA GRCh37
NC_000012.10:g.5998036_5998037delinsCA NCBI36
NG_009072.1:g.111061_111062delinsTG
NG_009072.2:g.111061_111062delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.4808_4809delinsTG MANE Select ENSP00000261405.5:p.Leu1603=
ENST00000261405.9:c.4808_4809delinsTG ENSP00000261405.5:p.Leu1603=
ENST00000538635.5:n.421-24676_421-24675delinsTG
NM_000552.3:c.4808_4809delinsTG NP_000543.2:p.Leu1603=
NM_000552.4:c.4808_4809delinsTG NP_000543.2:p.Leu1603=
NM_000552.5:c.4808_4809delinsTG MANE Select NP_000543.3:p.Leu1603=