Canonical Allele Identifier: CA2794398197

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6036124dup , CM000674.2:g.6036124dup	GRCh38
NC_000012.11:g.6145290dup , CM000674.1:g.6145290dup	GRCh37
NC_000012.10:g.6015551dup	NCBI36
NG_009072.1:g.93550dup
NG_009072.2:g.93550dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.2546+267dup MANE Select	ENSP00000261405.5:n.2546+267dup
ENST00000261405.9:c.2546+267dup	ENSP00000261405.5:n.2546+267dup
ENST00000538635.5:n.421-42187dup
NM_000552.3:c.2546+267dup	NP_000543.2:n.2546+267dup
NM_000552.4:c.2546+267dup	NP_000543.2:n.2546+267dup
NM_000552.5:c.2546+267dup MANE Select	NP_000543.3:n.2546+267dup