Canonical Allele Identifier: CA3341795

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90805341G>A , CM000667.2:g.90805341G>A	GRCh38
NC_000005.9:g.90101158G>A , CM000667.1:g.90101158G>A	GRCh37
NC_000005.8:g.90136914G>A	NCBI36
NG_007083.1:g.251542G>A
NG_007083.2:g.280998G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14719G>A MANE Select	NP_115495.3:p.Val4907Ile
ENST00000405460.9:c.14719G>A MANE Select	ENSP00000384582.2:p.Val4907Ile
NM_032119.3:c.14719G>A	NP_115495.3:p.Val4907Ile
NR_003149.1:n.14732G>A
NR_003149.2:n.14735G>A
ENST00000405460.6:c.14719G>A	ENSP00000384582.2:p.Val4907Ile
ENST00000425867.2:c.1702G>A	ENSP00000392618.2:p.Val568Ile
ENST00000425867.3:c.3673G>A	ENSP00000392618.3:p.Val1225Ile
ENST00000513828.1:n.415G>A
ENST00000638510.1:n.1986G>A
ENST00000638585.1:n.427+2459G>A
ENST00000639431.1:c.265+129132G>A	ENSP00000491057.1:n.265+129132G>A
ENST00000640407.1:c.1129G>A	ENSP00000491425.1:p.Val377Ile
XM_011543675.1:c.14716G>A	XP_011541977.1:p.Val4906Ile
XM_011543676.1:c.14638G>A	XP_011541978.1:p.Val4880Ile
XM_011543677.1:c.12022G>A	XP_011541979.1:p.Val4008Ile
XM_011543678.1:c.14719G>A	XP_011541980.1:p.Val4907Ile
XM_017009963.2:c.14740G>A	XP_016865452.1:p.Val4914Ile
XM_017009964.2:c.14737G>A	XP_016865453.1:p.Val4913Ile
XM_017009965.1:c.14737G>A	XP_016865454.1:p.Val4913Ile
XM_017009966.2:c.14659G>A	XP_016865455.1:p.Val4887Ile
XM_017009967.1:c.14644G>A	XP_016865456.1:p.Val4882Ile
XM_017009968.2:c.14683-2261G>A	XP_016865457.1:n.14683-2261G>A
XM_017009969.2:c.14740G>A	XP_016865458.1:p.Val4914Ile
XM_017009970.2:c.14740G>A	XP_016865459.1:p.Val4914Ile
XM_017009971.2:c.14683-2261G>A	XP_016865460.1:n.14683-2261G>A
XM_017009972.1:c.7858G>A	XP_016865461.1:p.Val2620Ile
XM_017009973.1:c.7837G>A	XP_016865462.1:p.Val2613Ile