Canonical Allele Identifier: CA2013880845

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036288_6036289delinsCA , CM000674.2:g.6036288_6036289delinsCA	GRCh38
NC_000012.11:g.6145454_6145455delinsCA , CM000674.1:g.6145454_6145455delinsCA	GRCh37
NC_000012.10:g.6015715_6015716delinsCA	NCBI36
NG_009072.1:g.93382_93383delinsTG
NG_009072.2:g.93382_93383delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261405.10:c.2546+99_2546+100delinsTG MANE Select	ENSP00000261405.5:n.2546+99_2546+100delinsTG
ENST00000261405.9:c.2546+99_2546+100delinsTG	ENSP00000261405.5:n.2546+99_2546+100delinsTG
ENST00000538635.5:n.421-42355_421-42354delinsTG
NM_000552.3:c.2546+99_2546+100delinsTG	NP_000543.2:n.2546+99_2546+100delinsTG
NM_000552.4:c.2546+99_2546+100delinsTG	NP_000543.2:n.2546+99_2546+100delinsTG
NM_000552.5:c.2546+99_2546+100delinsTG MANE Select	NP_000543.3:n.2546+99_2546+100delinsTG