Canonical Allele Identifier: CA2674570968
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755130dup , CM000667.2:g.90755130dup GRCh38
NC_000005.9:g.90050947dup , CM000667.1:g.90050947dup GRCh37
NC_000005.8:g.90086703dup NCBI36
NG_007083.1:g.201331dup
NG_007083.2:g.230787dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11525dup MANE Select ENSP00000384582.2:p.Ile3843AsnfsTer20
ENST00000425867.3:c.656dup ENSP00000392618.3:p.Ile220AsnfsTer28
ENST00000639431.1:c.265+78921dup ENSP00000491057.1:n.265+78921dup
ENST00000640374.1:n.4669dup
ENST00000640464.1:n.1944dup
ENST00000405460.6:c.11525dup ENSP00000384582.2:p.Ile3843AsnfsTer20
ENST00000509621.1:c.4222dup
NM_032119.3:c.11525dup NP_115495.3:p.Ile3843AsnfsTer20
NR_003149.1:n.11538dup
XM_011543675.1:c.11522dup XP_011541977.1:p.Ile3842AsnfsTer20
XM_011543676.1:c.11444dup XP_011541978.1:p.Ile3816AsnfsTer20
XM_011543677.1:c.8828dup XP_011541979.1:p.Ile2944AsnfsTer20
XM_011543678.1:c.11525dup XP_011541980.1:p.Ile3843AsnfsTer20
NM_032119.4:c.11525dup MANE Select NP_115495.3:p.Ile3843AsnfsTer20
XM_017009963.2:c.11546dup XP_016865452.1:p.Ile3850AsnfsTer20
XM_017009964.2:c.11543dup XP_016865453.1:p.Ile3849AsnfsTer20
XM_017009965.1:c.11543dup XP_016865454.1:p.Ile3849AsnfsTer20
XM_017009966.2:c.11465dup XP_016865455.1:p.Ile3823AsnfsTer20
XM_017009967.1:c.11450dup XP_016865456.1:p.Ile3818AsnfsTer20
XM_017009968.2:c.11546dup XP_016865457.1:p.Ile3850AsnfsTer20
XM_017009969.2:c.11546dup XP_016865458.1:p.Ile3850AsnfsTer20
XM_017009970.2:c.11546dup XP_016865459.1:p.Ile3850AsnfsTer20
XM_017009971.2:c.11546dup XP_016865460.1:p.Ile3850AsnfsTer20
XM_017009972.1:c.4664dup XP_016865461.1:p.Ile1556AsnfsTer20
XM_017009973.1:c.4643dup XP_016865462.1:p.Ile1549AsnfsTer20
NR_003149.2:n.11541dup