Canonical Allele Identifier: CA2674568335

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90728935-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728938_90728939del , CM000667.2:g.90728938_90728939del	GRCh38
NC_000005.9:g.90024755_90024756del , CM000667.1:g.90024755_90024756del	GRCh37
NC_000005.8:g.90060511_90060512del	NCBI36
NG_007083.1:g.175139_175140del
NG_007083.2:g.204595_204596del

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10426+5_10426+6del MANE Select	ENSP00000384582.2:n.10426+5_10426+6del
ENST00000639431.1:c.265+52729_265+52730del	ENSP00000491057.1:n.265+52729_265+52730de...
ENST00000640374.1:n.3570+5_3570+6del
ENST00000640464.1:n.845+5_845+6del
ENST00000405460.6:c.10426+5_10426+6del	ENSP00000384582.2:n.10426+5_10426+6del
ENST00000509621.1:c.3123+5_3123+6del
NM_032119.3:c.10426+5_10426+6del	NP_115495.3:n.10426+5_10426+6del
NR_003149.1:n.10439+5_10439+6del
XM_011543675.1:c.10423+5_10423+6del	XP_011541977.1:n.10423+5_10423+6del
XM_011543676.1:c.10345+5_10345+6del	XP_011541978.1:n.10345+5_10345+6del
XM_011543677.1:c.7729+5_7729+6del	XP_011541979.1:n.7729+5_7729+6del
XM_011543678.1:c.10426+5_10426+6del	XP_011541980.1:n.10426+5_10426+6del
XM_011543679.1:c.10426+5_10426+6del	XP_011541981.1:n.10426+5_10426+6del
XR_948560.1:n.271+11970_271+11971del
NM_032119.4:c.10426+5_10426+6del MANE Select	NP_115495.3:n.10426+5_10426+6del
XM_017009963.2:c.10447+5_10447+6del	XP_016865452.1:n.10447+5_10447+6del
XM_017009964.2:c.10444+5_10444+6del	XP_016865453.1:n.10444+5_10444+6del
XM_017009965.1:c.10444+5_10444+6del	XP_016865454.1:n.10444+5_10444+6del
XM_017009966.2:c.10366+5_10366+6del	XP_016865455.1:n.10366+5_10366+6del
XM_017009967.1:c.10351+5_10351+6del	XP_016865456.1:n.10351+5_10351+6del
XM_017009968.2:c.10447+5_10447+6del	XP_016865457.1:n.10447+5_10447+6del
XM_017009969.2:c.10447+5_10447+6del	XP_016865458.1:n.10447+5_10447+6del
XM_017009970.2:c.10447+5_10447+6del	XP_016865459.1:n.10447+5_10447+6del
XM_017009971.2:c.10447+5_10447+6del	XP_016865460.1:n.10447+5_10447+6del
XM_017009972.1:c.3565+5_3565+6del	XP_016865461.1:n.3565+5_3565+6del
XM_017009973.1:c.3544+5_3544+6del	XP_016865462.1:n.3544+5_3544+6del
XM_017009974.2:c.10447+5_10447+6del	XP_016865463.1:n.10447+5_10447+6del
XR_001742802.1:n.2522+11970_2522+11971del
NR_003149.2:n.10442+5_10442+6del