Canonical Allele Identifier: CA2013875065

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023899_6023902delinsTAGA , CM000674.2:g.6023899_6023902delinsTAGA	GRCh38
NC_000012.11:g.6133065_6133068delinsTAGA , CM000674.1:g.6133065_6133068delinsTAGA	GRCh37
NC_000012.10:g.6003326_6003329delinsTAGA	NCBI36
NG_009072.1:g.105769_105772delinsTCTA
NG_009072.2:g.105769_105772delinsTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-115_3223-112delinsTCTA MANE Select	ENSP00000261405.5:n.3223-115_3223-112delinsTCTA
ENST00000261405.9:c.3223-115_3223-112delinsTCTA	ENSP00000261405.5:n.3223-115_3223-112delinsTCTA
ENST00000538635.5:n.421-29968_421-29965delinsTCTA
NM_000552.3:c.3223-115_3223-112delinsTCTA	NP_000543.2:n.3223-115_3223-112delinsTCTA
NM_000552.4:c.3223-115_3223-112delinsTCTA	NP_000543.2:n.3223-115_3223-112delinsTCTA
NM_000552.5:c.3223-115_3223-112delinsTCTA MANE Select	NP_000543.3:n.3223-115_3223-112delinsTCTA