Canonical Allele Identifier: CA955346058

Gene: VWA8

Linked Data

• gnomAD v3: 13-41931575-TTGCC-T
• gnomAD v4: 13-41931575-TTGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.41931576_41931579del , CM000675.2:g.41931576_41931579del	GRCh38
NC_000013.10:g.42505712_42505715del , CM000675.1:g.42505712_42505715del	GRCh37
NC_000013.9:g.41403712_41403715del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379310.8:c.241+18357_241+18360del MANE Select	ENSP00000368612.3:n.241+18357_241+18360del
ENST00000281496.6:c.241+18357_241+18360del	ENSP00000281496.6:n.241+18357_241+18360del
ENST00000379310.7:c.241+18357_241+18360del	ENSP00000368612.3:n.241+18357_241+18360del
NM_001009814.1:c.241+18357_241+18360del	NP_001009814.1:n.241+18357_241+18360del
NM_015058.1:c.241+18357_241+18360del	NP_055873.1:n.241+18357_241+18360del
XM_011535006.1:c.-48+18357_-48+18360del	XP_011533308.1:n.-48+18357_-48+18360del
XM_011535007.1:c.241+18357_241+18360del	XP_011533309.1:n.241+18357_241+18360del
XM_011535007.3:c.241+18357_241+18360del	XP_011533309.1:n.241+18357_241+18360del
XM_017020469.2:c.58+5736_58+5739del	XP_016875958.1:n.58+5736_58+5739del
XM_017020470.2:c.241+18357_241+18360del	XP_016875959.1:n.241+18357_241+18360del
XM_017020471.2:c.241+18357_241+18360del	XP_016875960.1:n.241+18357_241+18360del
XM_017020474.2:c.241+18357_241+18360del	XP_016875963.1:n.241+18357_241+18360del
XR_001749518.2:n.972+18357_972+18360del
NM_015058.2:c.241+18357_241+18360del MANE Select	NP_055873.1:n.241+18357_241+18360del
NM_001009814.2:c.241+18357_241+18360del	NP_001009814.1:n.241+18357_241+18360del