Canonical Allele Identifier: CA2013875008

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023843_6023844delinsCT , CM000674.2:g.6023843_6023844delinsCT	GRCh38
NC_000012.11:g.6133009_6133010delinsCT , CM000674.1:g.6133009_6133010delinsCT	GRCh37
NC_000012.10:g.6003270_6003271delinsCT	NCBI36
NG_009072.1:g.105827_105828delinsAG
NG_009072.2:g.105827_105828delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-57_3223-56delinsAG MANE Select	ENSP00000261405.5:n.3223-57_3223-56delinsAG
ENST00000261405.9:c.3223-57_3223-56delinsAG	ENSP00000261405.5:n.3223-57_3223-56delinsAG
ENST00000538635.5:n.421-29910_421-29909delinsAG
NM_000552.3:c.3223-57_3223-56delinsAG	NP_000543.2:n.3223-57_3223-56delinsAG
NM_000552.4:c.3223-57_3223-56delinsAG	NP_000543.2:n.3223-57_3223-56delinsAG
NM_000552.5:c.3223-57_3223-56delinsAG MANE Select	NP_000543.3:n.3223-57_3223-56delinsAG