Canonical Allele Identifier: CA2674560134

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90617971-CCTTATAAAAATTATAAGGAGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617981_90618002del , CM000667.2:g.90617981_90618002del	GRCh38
NC_000005.9:g.89913798_89913819del , CM000667.1:g.89913798_89913819del	GRCh37
NC_000005.8:g.89949554_89949575del	NCBI36
NG_007083.1:g.64182_64203del
NG_007083.2:g.93638_93659del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.357+28_357+49del MANE Select	ENSP00000384582.2:n.357+28_357+49del
ENST00000638316.1:n.567+28_567+49del
ENST00000638638.1:n.764+28_764+49del
ENST00000640083.1:n.62+28_62+49del
ENST00000640109.1:n.453+28_453+49del
ENST00000640281.1:n.416+28_416+49del
ENST00000405460.6:c.357+28_357+49del	ENSP00000384582.2:n.357+28_357+49del
ENST00000508842.5:c.369+28_369+49del	ENSP00000425936.1:n.369+28_369+49del
NM_032119.3:c.357+28_357+49del	NP_115495.3:n.357+28_357+49del
NR_003149.1:n.453+28_453+49del
XM_011543675.1:c.357+28_357+49del	XP_011541977.1:n.357+28_357+49del
XM_011543676.1:c.357+28_357+49del	XP_011541978.1:n.357+28_357+49del
XM_011543678.1:c.357+28_357+49del	XP_011541980.1:n.357+28_357+49del
XM_011543679.1:c.357+28_357+49del	XP_011541981.1:n.357+28_357+49del
NM_032119.4:c.357+28_357+49del MANE Select	NP_115495.3:n.357+28_357+49del
XM_017009963.2:c.357+28_357+49del	XP_016865452.1:n.357+28_357+49del
XM_017009964.2:c.357+28_357+49del	XP_016865453.1:n.357+28_357+49del
XM_017009965.1:c.354+28_354+49del	XP_016865454.1:n.354+28_354+49del
XM_017009966.2:c.357+28_357+49del	XP_016865455.1:n.357+28_357+49del
XM_017009967.1:c.357+28_357+49del	XP_016865456.1:n.357+28_357+49del
XM_017009968.2:c.357+28_357+49del	XP_016865457.1:n.357+28_357+49del
XM_017009969.2:c.357+28_357+49del	XP_016865458.1:n.357+28_357+49del
XM_017009970.2:c.357+28_357+49del	XP_016865459.1:n.357+28_357+49del
XM_017009971.2:c.357+28_357+49del	XP_016865460.1:n.357+28_357+49del
XM_017009974.2:c.357+28_357+49del	XP_016865463.1:n.357+28_357+49del
NR_003149.2:n.456+28_456+49del