Canonical Allele Identifier: CA919013084

Gene: VWF

Linked Data

• dbSNP Id: rs1591865126

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6022131_6022143del , CM000674.2:g.6022131_6022143del	GRCh38
NC_000012.11:g.6131297_6131309del , CM000674.1:g.6131297_6131309del	GRCh37
NC_000012.10:g.6001558_6001570del	NCBI36
NG_009072.1:g.107530_107542del
NG_009072.2:g.107530_107542del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3539-106_3539-94del MANE Select	ENSP00000261405.5:n.3539-106_3539-94del
ENST00000261405.9:c.3539-106_3539-94del	ENSP00000261405.5:n.3539-106_3539-94del
ENST00000538635.5:n.421-28207_421-28195del
NM_000552.3:c.3539-106_3539-94del	NP_000543.2:n.3539-106_3539-94del
NM_000552.4:c.3539-106_3539-94del	NP_000543.2:n.3539-106_3539-94del
NM_000552.5:c.3539-106_3539-94del MANE Select	NP_000543.3:n.3539-106_3539-94del