Canonical Allele Identifier: CA2674568341

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90728946-AGTATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728950_90728955del , CM000667.2:g.90728950_90728955del	GRCh38
NC_000005.9:g.90024767_90024772del , CM000667.1:g.90024767_90024772del	GRCh37
NC_000005.8:g.90060523_90060528del	NCBI36
NG_007083.1:g.175151_175156del
NG_007083.2:g.204607_204612del

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10426+17_10426+22del MANE Select	ENSP00000384582.2:n.10426+17_10426+22del
ENST00000639431.1:c.265+52741_265+52746del	ENSP00000491057.1:n.265+52741_265+52746de...
ENST00000640374.1:n.3570+17_3570+22del
ENST00000640464.1:n.845+17_845+22del
ENST00000405460.6:c.10426+17_10426+22del	ENSP00000384582.2:n.10426+17_10426+22del
ENST00000509621.1:c.3123+17_3123+22del
NM_032119.3:c.10426+17_10426+22del	NP_115495.3:n.10426+17_10426+22del
NR_003149.1:n.10439+17_10439+22del
XM_011543675.1:c.10423+17_10423+22del	XP_011541977.1:n.10423+17_10423+22del
XM_011543676.1:c.10345+17_10345+22del	XP_011541978.1:n.10345+17_10345+22del
XM_011543677.1:c.7729+17_7729+22del	XP_011541979.1:n.7729+17_7729+22del
XM_011543678.1:c.10426+17_10426+22del	XP_011541980.1:n.10426+17_10426+22del
XM_011543679.1:c.10426+17_10426+22del	XP_011541981.1:n.10426+17_10426+22del
XR_948560.1:n.271+11955_271+11960del
NM_032119.4:c.10426+17_10426+22del MANE Select	NP_115495.3:n.10426+17_10426+22del
XM_017009963.2:c.10447+17_10447+22del	XP_016865452.1:n.10447+17_10447+22del
XM_017009964.2:c.10444+17_10444+22del	XP_016865453.1:n.10444+17_10444+22del
XM_017009965.1:c.10444+17_10444+22del	XP_016865454.1:n.10444+17_10444+22del
XM_017009966.2:c.10366+17_10366+22del	XP_016865455.1:n.10366+17_10366+22del
XM_017009967.1:c.10351+17_10351+22del	XP_016865456.1:n.10351+17_10351+22del
XM_017009968.2:c.10447+17_10447+22del	XP_016865457.1:n.10447+17_10447+22del
XM_017009969.2:c.10447+17_10447+22del	XP_016865458.1:n.10447+17_10447+22del
XM_017009970.2:c.10447+17_10447+22del	XP_016865459.1:n.10447+17_10447+22del
XM_017009971.2:c.10447+17_10447+22del	XP_016865460.1:n.10447+17_10447+22del
XM_017009972.1:c.3565+17_3565+22del	XP_016865461.1:n.3565+17_3565+22del
XM_017009973.1:c.3544+17_3544+22del	XP_016865462.1:n.3544+17_3544+22del
XM_017009974.2:c.10447+17_10447+22del	XP_016865463.1:n.10447+17_10447+22del
XR_001742802.1:n.2522+11955_2522+11960del
NR_003149.2:n.10442+17_10442+22del