Canonical Allele Identifier: CA2013875094

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023929_6023931delinsAAG , CM000674.2:g.6023929_6023931delinsAAG	GRCh38
NC_000012.11:g.6133095_6133097delinsAAG , CM000674.1:g.6133095_6133097delinsAAG	GRCh37
NC_000012.10:g.6003356_6003358delinsAAG	NCBI36
NG_009072.1:g.105740_105742delinsCTT
NG_009072.2:g.105740_105742delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-144_3223-142delinsCTT MANE Select	ENSP00000261405.5:n.3223-144_3223-142delinsCTT
ENST00000261405.9:c.3223-144_3223-142delinsCTT	ENSP00000261405.5:n.3223-144_3223-142delinsCTT
ENST00000538635.5:n.421-29997_421-29995delinsCTT
NM_000552.3:c.3223-144_3223-142delinsCTT	NP_000543.2:n.3223-144_3223-142delinsCTT
NM_000552.4:c.3223-144_3223-142delinsCTT	NP_000543.2:n.3223-144_3223-142delinsCTT
NM_000552.5:c.3223-144_3223-142delinsCTT MANE Select	NP_000543.3:n.3223-144_3223-142delinsCTT