Canonical Allele Identifier: CA2013872462

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6018336_6018337delinsTC , CM000674.2:g.6018336_6018337delinsTC	GRCh38
NC_000012.11:g.6127502_6127503delinsTC , CM000674.1:g.6127502_6127503delinsTC	GRCh37
NC_000012.10:g.5997763_5997764delinsTC	NCBI36
NG_009072.1:g.111334_111335delinsGA
NG_009072.2:g.111334_111335delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.5053+28_5053+29delinsGA MANE Select	ENSP00000261405.5:n.5053+28_5053+29delinsGA
ENST00000261405.9:c.5053+28_5053+29delinsGA	ENSP00000261405.5:n.5053+28_5053+29delinsGA
ENST00000538635.5:n.421-24403_421-24402delinsGA
NM_000552.3:c.5053+28_5053+29delinsGA	NP_000543.2:n.5053+28_5053+29delinsGA
NM_000552.4:c.5053+28_5053+29delinsGA	NP_000543.2:n.5053+28_5053+29delinsGA
NM_000552.5:c.5053+28_5053+29delinsGA MANE Select	NP_000543.3:n.5053+28_5053+29delinsGA