Canonical Allele Identifier: CA2013874722

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023326_6023330delinsCTAAT , CM000674.2:g.6023326_6023330delinsCTAAT	GRCh38
NC_000012.11:g.6132492_6132496delinsCTAAT , CM000674.1:g.6132492_6132496delinsCTAAT	GRCh37
NC_000012.10:g.6002753_6002757delinsCTAAT	NCBI36
NG_009072.1:g.106341_106345delinsATTAG
NG_009072.2:g.106341_106345delinsATTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3379+301_3379+305delinsATTAG MANE Select	ENSP00000261405.5:n.3379+301_3379+305delinsATTAG
ENST00000261405.9:c.3379+301_3379+305delinsATTAG	ENSP00000261405.5:n.3379+301_3379+305delinsATTAG
ENST00000538635.5:n.421-29396_421-29392delinsATTAG
NM_000552.3:c.3379+301_3379+305delinsATTAG	NP_000543.2:n.3379+301_3379+305delinsATTAG
NM_000552.4:c.3379+301_3379+305delinsATTAG	NP_000543.2:n.3379+301_3379+305delinsATTAG
NM_000552.5:c.3379+301_3379+305delinsATTAG MANE Select	NP_000543.3:n.3379+301_3379+305delinsATTAG