Canonical Allele Identifier: CA2695216055

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023773del , CM000674.2:g.6023773del	GRCh38
NC_000012.11:g.6132939del , CM000674.1:g.6132939del	GRCh37
NC_000012.10:g.6003200del	NCBI36
NG_009072.1:g.105898del
NG_009072.2:g.105898del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3237del MANE Select	ENSP00000261405.5:p.Tyr1080IlefsTer?
ENST00000261405.9:c.3237del	ENSP00000261405.5:p.Tyr1080IlefsTer?
ENST00000538635.5:n.421-29839del
NM_000552.3:c.3237del	NP_000543.2:p.Tyr1080IlefsTer?
NM_000552.4:c.3237del	NP_000543.2:p.Tyr1080IlefsTer?
NM_000552.5:c.3237del MANE Select	NP_000543.3:p.Tyr1080IlefsTer?