Canonical Allele Identifier: CA2013892406
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6058144_6058145delinsCG , CM000674.2:g.6058144_6058145delinsCG GRCh38
NC_000012.11:g.6167310_6167311delinsCG , CM000674.1:g.6167310_6167311delinsCG GRCh37
NC_000012.10:g.6037571_6037572delinsCG NCBI36
NG_009072.1:g.71526_71527delinsCG
NG_009072.2:g.71526_71527delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.1534-101_1534-100delinsCG MANE Select ENSP00000261405.5:n.1534-101_1534-100delinsCG
ENST00000261405.9:c.1534-101_1534-100delinsCG ENSP00000261405.5:n.1534-101_1534-100delinsCG
ENST00000538635.5:n.420+52370_420+52371delinsCG
NM_000552.3:c.1534-101_1534-100delinsCG NP_000543.2:n.1534-101_1534-100delinsCG
NM_000552.4:c.1534-101_1534-100delinsCG NP_000543.2:n.1534-101_1534-100delinsCG
NM_000552.5:c.1534-101_1534-100delinsCG MANE Select NP_000543.3:n.1534-101_1534-100delinsCG