Canonical Allele Identifier: CA2617230406

Gene: VWF

Linked Data

• gnomAD v4: 12-6023805-G-GCCTCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6023805_6023806insCCTCAA , CM000674.2:g.6023805_6023806insCCTCAA	GRCh38
NC_000012.11:g.6132971_6132972insCCTCAA , CM000674.1:g.6132971_6132972insCCTCAA	GRCh37
NC_000012.10:g.6003232_6003233insCCTCAA	NCBI36
NG_009072.1:g.105865_105866insTTGAGG
NG_009072.2:g.105865_105866insTTGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3223-19_3223-18insTTGAGG MANE Select	ENSP00000261405.5:n.3223-19_3223-18insTTGAGG
ENST00000261405.9:c.3223-19_3223-18insTTGAGG	ENSP00000261405.5:n.3223-19_3223-18insTTGAGG
ENST00000538635.5:n.421-29872_421-29871insTTGAGG
NM_000552.3:c.3223-19_3223-18insTTGAGG	NP_000543.2:n.3223-19_3223-18insTTGAGG
NM_000552.4:c.3223-19_3223-18insTTGAGG	NP_000543.2:n.3223-19_3223-18insTTGAGG
NM_000552.5:c.3223-19_3223-18insTTGAGG MANE Select	NP_000543.3:n.3223-19_3223-18insTTGAGG