Canonical Allele Identifier: CA1562825076

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617964_90617981delinsGTTTCCTCCTTATAAAAA , CM000667.2:g.90617964_90617981delinsGTTTCCTCCTTATAAAAA	GRCh38
NC_000005.9:g.89913781_89913798delinsGTTTCCTCCTTATAAAAA , CM000667.1:g.89913781_89913798delinsGTTTCCTCCTTATAAAAA	GRCh37
NC_000005.8:g.89949537_89949554delinsGTTTCCTCCTTATAAAAA	NCBI36
NG_007083.1:g.64165_64182delinsGTTTCCTCCTTATAAAAA
NG_007083.2:g.93621_93638delinsGTTTCCTCCTTATAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA MANE Select	ENSP00000384582.2:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
ENST00000638316.1:n.567+11_567+28delinsGTTTCCTCCTTATAAAAA
ENST00000638638.1:n.764+11_764+28delinsGTTTCCTCCTTATAAAAA
ENST00000640083.1:n.62+11_62+28delinsGTTTCCTCCTTATAAAAA
ENST00000640109.1:n.453+11_453+28delinsGTTTCCTCCTTATAAAAA
ENST00000640281.1:n.416+11_416+28delinsGTTTCCTCCTTATAAAAA
ENST00000405460.6:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	ENSP00000384582.2:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
ENST00000508842.5:c.369+11_369+28delinsGTTTCCTCCTTATAAAAA	ENSP00000425936.1:n.369+11_369+28delinsGTTTCCTCCTTATAAAAA
NM_032119.3:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	NP_115495.3:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
NR_003149.1:n.453+11_453+28delinsGTTTCCTCCTTATAAAAA
XM_011543675.1:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_011541977.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_011543676.1:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_011541978.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_011543678.1:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_011541980.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_011543679.1:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_011541981.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
NM_032119.4:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA MANE Select	NP_115495.3:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009963.2:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865452.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009964.2:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865453.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009965.1:c.354+11_354+28delinsGTTTCCTCCTTATAAAAA	XP_016865454.1:n.354+11_354+28delinsGTTTCCTCCTTATAAAAA
XM_017009966.2:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865455.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009967.1:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865456.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009968.2:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865457.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009969.2:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865458.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009970.2:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865459.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009971.2:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865460.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
XM_017009974.2:c.357+11_357+28delinsGTTTCCTCCTTATAAAAA	XP_016865463.1:n.357+11_357+28delinsGTTTCCTCCTTATAAAAA
NR_003149.2:n.456+11_456+28delinsGTTTCCTCCTTATAAAAA