Canonical Allele Identifier: CA2013876859

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6031637_6031638delinsGA , CM000674.2:g.6031637_6031638delinsGA	GRCh38
NC_000012.11:g.6140803_6140804delinsGA , CM000674.1:g.6140803_6140804delinsGA	GRCh37
NC_000012.10:g.6011064_6011065delinsGA	NCBI36
NG_009072.1:g.98033_98034delinsTC
NG_009072.2:g.98033_98034delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2686-60_2686-59delinsTC MANE Select	ENSP00000261405.5:n.2686-60_2686-59delinsTC
ENST00000261405.9:c.2686-60_2686-59delinsTC	ENSP00000261405.5:n.2686-60_2686-59delinsTC
ENST00000538635.5:n.421-37704_421-37703delinsTC
NM_000552.3:c.2686-60_2686-59delinsTC	NP_000543.2:n.2686-60_2686-59delinsTC
NM_000552.4:c.2686-60_2686-59delinsTC	NP_000543.2:n.2686-60_2686-59delinsTC
NM_000552.5:c.2686-60_2686-59delinsTC MANE Select	NP_000543.3:n.2686-60_2686-59delinsTC