Canonical Allele Identifier: CA1562886222
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755136_90755137delinsTA , CM000667.2:g.90755136_90755137delinsTA GRCh38
NC_000005.9:g.90050953_90050954delinsTA , CM000667.1:g.90050953_90050954delinsTA GRCh37
NC_000005.8:g.90086709_90086710delinsTA NCBI36
NG_007083.1:g.201337_201338delinsTA
NG_007083.2:g.230793_230794delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11531_11532delinsTA MANE Select ENSP00000384582.2:p.Ile3844=
ENST00000425867.3:c.662_663delinsTA ENSP00000392618.3:p.Ile221=
ENST00000639431.1:c.265+78927_265+78928delinsTA ENSP00000491057.1:n.265+78927_265+78928delinsTA
ENST00000640374.1:n.4675_4676delinsTA
ENST00000640464.1:n.1950_1951delinsTA
ENST00000405460.6:c.11531_11532delinsTA ENSP00000384582.2:p.Ile3844=
ENST00000509621.1:c.4228_4229delinsTA
NM_032119.3:c.11531_11532delinsTA NP_115495.3:p.Ile3844=
NR_003149.1:n.11544_11545delinsTA
XM_011543675.1:c.11528_11529delinsTA XP_011541977.1:p.Ile3843=
XM_011543676.1:c.11450_11451delinsTA XP_011541978.1:p.Ile3817=
XM_011543677.1:c.8834_8835delinsTA XP_011541979.1:p.Ile2945=
XM_011543678.1:c.11531_11532delinsTA XP_011541980.1:p.Ile3844=
NM_032119.4:c.11531_11532delinsTA MANE Select NP_115495.3:p.Ile3844=
XM_017009963.2:c.11552_11553delinsTA XP_016865452.1:p.Ile3851=
XM_017009964.2:c.11549_11550delinsTA XP_016865453.1:p.Ile3850=
XM_017009965.1:c.11549_11550delinsTA XP_016865454.1:p.Ile3850=
XM_017009966.2:c.11471_11472delinsTA XP_016865455.1:p.Ile3824=
XM_017009967.1:c.11456_11457delinsTA XP_016865456.1:p.Ile3819=
XM_017009968.2:c.11552_11553delinsTA XP_016865457.1:p.Ile3851=
XM_017009969.2:c.11552_11553delinsTA XP_016865458.1:p.Ile3851=
XM_017009970.2:c.11552_11553delinsTA XP_016865459.1:p.Ile3851=
XM_017009971.2:c.11552_11553delinsTA XP_016865460.1:p.Ile3851=
XM_017009972.1:c.4670_4671delinsTA XP_016865461.1:p.Ile1557=
XM_017009973.1:c.4649_4650delinsTA XP_016865462.1:p.Ile1550=
NR_003149.2:n.11547_11548delinsTA