Canonical Allele Identifier: CA2013874909
Gene: VWF HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6023739_6023740delinsAG , CM000674.2:g.6023739_6023740delinsAG GRCh38
NC_000012.11:g.6132905_6132906delinsAG , CM000674.1:g.6132905_6132906delinsAG GRCh37
NC_000012.10:g.6003166_6003167delinsAG NCBI36
NG_009072.1:g.105931_105932delinsCT
NG_009072.2:g.105931_105932delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.3270_3271delinsCT MANE Select ENSP00000261405.5:p.Ser1090=
ENST00000261405.9:c.3270_3271delinsCT ENSP00000261405.5:p.Ser1090=
ENST00000538635.5:n.421-29806_421-29805delinsCT
NM_000552.3:c.3270_3271delinsCT NP_000543.2:p.Ser1090=
NM_000552.4:c.3270_3271delinsCT NP_000543.2:p.Ser1090=
NM_000552.5:c.3270_3271delinsCT MANE Select NP_000543.3:p.Ser1090=
Search 100 bp 5'
Search 100 bp 3'