Canonical Allele Identifier: CA3339279

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90653570A>G , CM000667.2:g.90653570A>G	GRCh38
NC_000005.9:g.89949387A>G , CM000667.1:g.89949387A>G	GRCh37
NC_000005.8:g.89985143A>G	NCBI36
NG_007083.1:g.99771A>G
NG_007083.2:g.129227A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.3996A>G MANE Select	NP_115495.3:p.Gly1332=
ENST00000405460.9:c.3996A>G MANE Select	ENSP00000384582.2:p.Gly1332=
NM_032119.3:c.3996A>G	NP_115495.3:p.Gly1332=
NR_003149.1:n.4092A>G
NR_003149.2:n.4095A>G
ENST00000405460.6:c.3996A>G	ENSP00000384582.2:p.Gly1332=
ENST00000504142.1:c.2761A>G
ENST00000504142.2:n.2762A>G
ENST00000639676.1:n.1594A>G
ENST00000640403.1:c.1287A>G	ENSP00000492531.1:p.Gly429=
XM_011543675.1:c.3996A>G	XP_011541977.1:p.Gly1332=
XM_011543676.1:c.3996A>G	XP_011541978.1:p.Gly1332=
XM_011543677.1:c.1299A>G	XP_011541979.1:p.Gly433=
XM_011543678.1:c.3996A>G	XP_011541980.1:p.Gly1332=
XM_011543679.1:c.3996A>G	XP_011541981.1:p.Gly1332=
XM_017009963.2:c.3996A>G	XP_016865452.1:p.Gly1332=
XM_017009964.2:c.3996A>G	XP_016865453.1:p.Gly1332=
XM_017009965.1:c.3993A>G	XP_016865454.1:p.Gly1331=
XM_017009966.2:c.3996A>G	XP_016865455.1:p.Gly1332=
XM_017009967.1:c.3900A>G	XP_016865456.1:p.Gly1300=
XM_017009968.2:c.3996A>G	XP_016865457.1:p.Gly1332=
XM_017009969.2:c.3996A>G	XP_016865458.1:p.Gly1332=
XM_017009970.2:c.3996A>G	XP_016865459.1:p.Gly1332=
XM_017009971.2:c.3996A>G	XP_016865460.1:p.Gly1332=
XM_017009974.2:c.3996A>G	XP_016865463.1:p.Gly1332=