Canonical Allele Identifier: CA1562825036
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90617864G= , CM000667.2:g.90617864G= GRCh38
NC_000005.9:g.89913681G= , CM000667.1:g.89913681G= GRCh37
NC_000005.8:g.89949437G= NCBI36
NG_007083.1:g.64065G=
NG_007083.2:g.93521G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.268G= MANE Select ENSP00000384582.2:p.Gly90=
ENST00000638316.1:n.478G=
ENST00000638638.1:n.675G=
ENST00000640109.1:n.364G=
ENST00000640281.1:n.327G=
ENST00000405460.6:c.268G= ENSP00000384582.2:p.Gly90=
ENST00000508842.5:c.280G= ENSP00000425936.1:p.Gly94=
NM_032119.3:c.268G= NP_115495.3:p.Gly90=
NR_003149.1:n.364G=
XM_011543675.1:c.268G= XP_011541977.1:p.Gly90=
XM_011543676.1:c.268G= XP_011541978.1:p.Gly90=
XM_011543678.1:c.268G= XP_011541980.1:p.Gly90=
XM_011543679.1:c.268G= XP_011541981.1:p.Gly90=
NM_032119.4:c.268G= MANE Select NP_115495.3:p.Gly90=
XM_017009963.2:c.268G= XP_016865452.1:p.Gly90=
XM_017009964.2:c.268G= XP_016865453.1:p.Gly90=
XM_017009965.1:c.265G= XP_016865454.1:p.Gly89=
XM_017009966.2:c.268G= XP_016865455.1:p.Gly90=
XM_017009967.1:c.268G= XP_016865456.1:p.Gly90=
XM_017009968.2:c.268G= XP_016865457.1:p.Gly90=
XM_017009969.2:c.268G= XP_016865458.1:p.Gly90=
XM_017009970.2:c.268G= XP_016865459.1:p.Gly90=
XM_017009971.2:c.268G= XP_016865460.1:p.Gly90=
XM_017009974.2:c.268G= XP_016865463.1:p.Gly90=
NR_003149.2:n.367G=