Canonical Allele Identifier: CA1562825211
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90618254_90618255delinsCT , CM000667.2:g.90618254_90618255delinsCT GRCh38
NC_000005.9:g.89914071_89914072delinsCT , CM000667.1:g.89914071_89914072delinsCT GRCh37
NC_000005.8:g.89949827_89949828delinsCT NCBI36
NG_007083.1:g.64455_64456delinsCT
NG_007083.2:g.93911_93912delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.357+301_357+302delinsCT MANE Select ENSP00000384582.2:n.357+301_357+302delinsCT
ENST00000638316.1:n.567+301_567+302delinsCT
ENST00000638638.1:n.764+301_764+302delinsCT
ENST00000640083.1:n.62+301_62+302delinsCT
ENST00000640109.1:n.453+301_453+302delinsCT
ENST00000640281.1:n.416+301_416+302delinsCT
ENST00000405460.6:c.357+301_357+302delinsCT ENSP00000384582.2:n.357+301_357+302delinsCT
ENST00000508842.5:c.369+301_369+302delinsCT ENSP00000425936.1:n.369+301_369+302delinsCT
NM_032119.3:c.357+301_357+302delinsCT NP_115495.3:n.357+301_357+302delinsCT
NR_003149.1:n.453+301_453+302delinsCT
XM_011543675.1:c.357+301_357+302delinsCT XP_011541977.1:n.357+301_357+302delinsCT
XM_011543676.1:c.357+301_357+302delinsCT XP_011541978.1:n.357+301_357+302delinsCT
XM_011543678.1:c.357+301_357+302delinsCT XP_011541980.1:n.357+301_357+302delinsCT
XM_011543679.1:c.357+301_357+302delinsCT XP_011541981.1:n.357+301_357+302delinsCT
NM_032119.4:c.357+301_357+302delinsCT MANE Select NP_115495.3:n.357+301_357+302delinsCT
XM_017009963.2:c.357+301_357+302delinsCT XP_016865452.1:n.357+301_357+302delinsCT
XM_017009964.2:c.357+301_357+302delinsCT XP_016865453.1:n.357+301_357+302delinsCT
XM_017009965.1:c.354+301_354+302delinsCT XP_016865454.1:n.354+301_354+302delinsCT
XM_017009966.2:c.357+301_357+302delinsCT XP_016865455.1:n.357+301_357+302delinsCT
XM_017009967.1:c.357+301_357+302delinsCT XP_016865456.1:n.357+301_357+302delinsCT
XM_017009968.2:c.357+301_357+302delinsCT XP_016865457.1:n.357+301_357+302delinsCT
XM_017009969.2:c.357+301_357+302delinsCT XP_016865458.1:n.357+301_357+302delinsCT
XM_017009970.2:c.357+301_357+302delinsCT XP_016865459.1:n.357+301_357+302delinsCT
XM_017009971.2:c.357+301_357+302delinsCT XP_016865460.1:n.357+301_357+302delinsCT
XM_017009974.2:c.357+301_357+302delinsCT XP_016865463.1:n.357+301_357+302delinsCT
NR_003149.2:n.456+301_456+302delinsCT