Canonical Allele Identifier: CA2767415139
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90617966_90617967insACAG , CM000667.2:g.90617966_90617967insACAG GRCh38
NC_000005.9:g.89913783_89913784insACAG , CM000667.1:g.89913783_89913784insACAG GRCh37
NC_000005.8:g.89949539_89949540insACAG NCBI36
NG_007083.1:g.64167_64168insACAG
NG_007083.2:g.93623_93624insACAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.357+13_357+14insACAG MANE Select ENSP00000384582.2:n.357+13_357+14insACAG
ENST00000638316.1:n.567+13_567+14insACAG
ENST00000638638.1:n.764+13_764+14insACAG
ENST00000640083.1:n.62+13_62+14insACAG
ENST00000640109.1:n.453+13_453+14insACAG
ENST00000640281.1:n.416+13_416+14insACAG
ENST00000405460.6:c.357+13_357+14insACAG ENSP00000384582.2:n.357+13_357+14insACAG
ENST00000508842.5:c.369+13_369+14insACAG ENSP00000425936.1:n.369+13_369+14insACAG
NM_032119.3:c.357+13_357+14insACAG NP_115495.3:n.357+13_357+14insACAG
NR_003149.1:n.453+13_453+14insACAG
XM_011543675.1:c.357+13_357+14insACAG XP_011541977.1:n.357+13_357+14insACAG
XM_011543676.1:c.357+13_357+14insACAG XP_011541978.1:n.357+13_357+14insACAG
XM_011543678.1:c.357+13_357+14insACAG XP_011541980.1:n.357+13_357+14insACAG
XM_011543679.1:c.357+13_357+14insACAG XP_011541981.1:n.357+13_357+14insACAG
NM_032119.4:c.357+13_357+14insACAG MANE Select NP_115495.3:n.357+13_357+14insACAG
XM_017009963.2:c.357+13_357+14insACAG XP_016865452.1:n.357+13_357+14insACAG
XM_017009964.2:c.357+13_357+14insACAG XP_016865453.1:n.357+13_357+14insACAG
XM_017009965.1:c.354+13_354+14insACAG XP_016865454.1:n.354+13_354+14insACAG
XM_017009966.2:c.357+13_357+14insACAG XP_016865455.1:n.357+13_357+14insACAG
XM_017009967.1:c.357+13_357+14insACAG XP_016865456.1:n.357+13_357+14insACAG
XM_017009968.2:c.357+13_357+14insACAG XP_016865457.1:n.357+13_357+14insACAG
XM_017009969.2:c.357+13_357+14insACAG XP_016865458.1:n.357+13_357+14insACAG
XM_017009970.2:c.357+13_357+14insACAG XP_016865459.1:n.357+13_357+14insACAG
XM_017009971.2:c.357+13_357+14insACAG XP_016865460.1:n.357+13_357+14insACAG
XM_017009974.2:c.357+13_357+14insACAG XP_016865463.1:n.357+13_357+14insACAG
NR_003149.2:n.456+13_456+14insACAG