Canonical Allele Identifier: CA3340965

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90754990C>G , CM000667.2:g.90754990C>G	GRCh38
NC_000005.9:g.90050807C>G , CM000667.1:g.90050807C>G	GRCh37
NC_000005.8:g.90086563C>G	NCBI36
NG_007083.1:g.201191C>G
NG_007083.2:g.230647C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11385C>G MANE Select	NP_115495.3:p.Thr3795=
ENST00000405460.9:c.11385C>G MANE Select	ENSP00000384582.2:p.Thr3795=
NM_032119.3:c.11385C>G	NP_115495.3:p.Thr3795=
NR_003149.1:n.11398C>G
NR_003149.2:n.11401C>G
ENST00000405460.6:c.11385C>G	ENSP00000384582.2:p.Thr3795=
ENST00000425867.3:c.516C>G	ENSP00000392618.3:p.Thr172=
ENST00000509621.1:c.4082C>G
ENST00000639431.1:c.265+78781C>G	ENSP00000491057.1:n.265+78781C>G
ENST00000640374.1:n.4529C>G
ENST00000640464.1:n.1804C>G
XM_011543675.1:c.11382C>G	XP_011541977.1:p.Thr3794=
XM_011543676.1:c.11304C>G	XP_011541978.1:p.Thr3768=
XM_011543677.1:c.8688C>G	XP_011541979.1:p.Thr2896=
XM_011543678.1:c.11385C>G	XP_011541980.1:p.Thr3795=
XM_017009963.2:c.11406C>G	XP_016865452.1:p.Thr3802=
XM_017009964.2:c.11403C>G	XP_016865453.1:p.Thr3801=
XM_017009965.1:c.11403C>G	XP_016865454.1:p.Thr3801=
XM_017009966.2:c.11325C>G	XP_016865455.1:p.Thr3775=
XM_017009967.1:c.11310C>G	XP_016865456.1:p.Thr3770=
XM_017009968.2:c.11406C>G	XP_016865457.1:p.Thr3802=
XM_017009969.2:c.11406C>G	XP_016865458.1:p.Thr3802=
XM_017009970.2:c.11406C>G	XP_016865459.1:p.Thr3802=
XM_017009971.2:c.11406C>G	XP_016865460.1:p.Thr3802=
XM_017009972.1:c.4524C>G	XP_016865461.1:p.Thr1508=
XM_017009973.1:c.4503C>G	XP_016865462.1:p.Thr1501=