Canonical Allele Identifier: CA955346059
Gene: VWA8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.41931583_41931584del , CM000675.2:g.41931583_41931584del GRCh38
NC_000013.10:g.42505719_42505720del , CM000675.1:g.42505719_42505720del GRCh37
NC_000013.9:g.41403719_41403720del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379310.8:c.241+18352_241+18353del MANE Select ENSP00000368612.3:n.241+18352_241+18353de...
ENST00000281496.6:c.241+18352_241+18353del ENSP00000281496.6:n.241+18352_241+18353de...
ENST00000379310.7:c.241+18352_241+18353del ENSP00000368612.3:n.241+18352_241+18353de...
NM_001009814.1:c.241+18352_241+18353del NP_001009814.1:n.241+18352_241+18353del
NM_015058.1:c.241+18352_241+18353del NP_055873.1:n.241+18352_241+18353del
XM_011535006.1:c.-48+18352_-48+18353del XP_011533308.1:n.-48+18352_-48+18353del
XM_011535007.1:c.241+18352_241+18353del XP_011533309.1:n.241+18352_241+18353del
XM_011535007.3:c.241+18352_241+18353del XP_011533309.1:n.241+18352_241+18353del
XM_017020469.2:c.58+5731_58+5732del XP_016875958.1:n.58+5731_58+5732del
XM_017020470.2:c.241+18352_241+18353del XP_016875959.1:n.241+18352_241+18353del
XM_017020471.2:c.241+18352_241+18353del XP_016875960.1:n.241+18352_241+18353del
XM_017020474.2:c.241+18352_241+18353del XP_016875963.1:n.241+18352_241+18353del
XR_001749518.2:n.972+18352_972+18353del
NM_015058.2:c.241+18352_241+18353del MANE Select NP_055873.1:n.241+18352_241+18353del
NM_001009814.2:c.241+18352_241+18353del NP_001009814.1:n.241+18352_241+18353del