Canonical Allele Identifier: CA955346066

Gene: VWA8

Linked Data

• dbSNP Id: rs754167381
• gnomAD v3: 13-41931584-CA-C
• gnomAD v4: 13-41931584-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.41931592del , CM000675.2:g.41931592del	GRCh38
NC_000013.10:g.42505728del , CM000675.1:g.42505728del	GRCh37
NC_000013.9:g.41403728del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379310.8:c.241+18351del MANE Select	ENSP00000368612.3:n.241+18351del
ENST00000281496.6:c.241+18351del	ENSP00000281496.6:n.241+18351del
ENST00000379310.7:c.241+18351del	ENSP00000368612.3:n.241+18351del
NM_001009814.1:c.241+18351del	NP_001009814.1:n.241+18351del
NM_015058.1:c.241+18351del	NP_055873.1:n.241+18351del
XM_011535006.1:c.-48+18351del	XP_011533308.1:n.-48+18351del
XM_011535007.1:c.241+18351del	XP_011533309.1:n.241+18351del
XM_011535007.3:c.241+18351del	XP_011533309.1:n.241+18351del
XM_017020469.2:c.58+5730del	XP_016875958.1:n.58+5730del
XM_017020470.2:c.241+18351del	XP_016875959.1:n.241+18351del
XM_017020471.2:c.241+18351del	XP_016875960.1:n.241+18351del
XM_017020474.2:c.241+18351del	XP_016875963.1:n.241+18351del
XR_001749518.2:n.972+18351del
NM_015058.2:c.241+18351del MANE Select	NP_055873.1:n.241+18351del
NM_001009814.2:c.241+18351del	NP_001009814.1:n.241+18351del