Canonical Allele Identifier: CA1562886227
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755151_90755155delinsTAAAA , CM000667.2:g.90755151_90755155delinsTAAAA GRCh38
NC_000005.9:g.90050968_90050972delinsTAAAA , CM000667.1:g.90050968_90050972delinsTAAAA GRCh37
NC_000005.8:g.90086724_90086728delinsTAAAA NCBI36
NG_007083.1:g.201352_201356delinsTAAAA
NG_007083.2:g.230808_230812delinsTAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11546_11550delinsTAAAA MANE Select ENSP00000384582.2:p.Ile3849=
ENST00000425867.3:c.677_681delinsTAAAA ENSP00000392618.3:p.Ile226=
ENST00000639431.1:c.265+78942_265+78946delinsTAAAA ENSP00000491057.1:n.265+78942_265+78946delinsTAAAA
ENST00000640374.1:n.4690_4694delinsTAAAA
ENST00000640464.1:n.1965_1969delinsTAAAA
ENST00000405460.6:c.11546_11550delinsTAAAA ENSP00000384582.2:p.Ile3849=
ENST00000509621.1:c.4243_4247delinsTAAAA
NM_032119.3:c.11546_11550delinsTAAAA NP_115495.3:p.Ile3849=
NR_003149.1:n.11559_11563delinsTAAAA
XM_011543675.1:c.11543_11547delinsTAAAA XP_011541977.1:p.Ile3848=
XM_011543676.1:c.11465_11469delinsTAAAA XP_011541978.1:p.Ile3822=
XM_011543677.1:c.8849_8853delinsTAAAA XP_011541979.1:p.Ile2950=
XM_011543678.1:c.11546_11550delinsTAAAA XP_011541980.1:p.Ile3849=
NM_032119.4:c.11546_11550delinsTAAAA MANE Select NP_115495.3:p.Ile3849=
XM_017009963.2:c.11567_11571delinsTAAAA XP_016865452.1:p.Ile3856=
XM_017009964.2:c.11564_11568delinsTAAAA XP_016865453.1:p.Ile3855=
XM_017009965.1:c.11564_11568delinsTAAAA XP_016865454.1:p.Ile3855=
XM_017009966.2:c.11486_11490delinsTAAAA XP_016865455.1:p.Ile3829=
XM_017009967.1:c.11471_11475delinsTAAAA XP_016865456.1:p.Ile3824=
XM_017009968.2:c.11567_11571delinsTAAAA XP_016865457.1:p.Ile3856=
XM_017009969.2:c.11567_11571delinsTAAAA XP_016865458.1:p.Ile3856=
XM_017009970.2:c.11567_11571delinsTAAAA XP_016865459.1:p.Ile3856=
XM_017009971.2:c.11567_11571delinsTAAAA XP_016865460.1:p.Ile3856=
XM_017009972.1:c.4685_4689delinsTAAAA XP_016865461.1:p.Ile1562=
XM_017009973.1:c.4664_4668delinsTAAAA XP_016865462.1:p.Ile1555=
NR_003149.2:n.11562_11566delinsTAAAA