Canonical Allele Identifier: CA3341711

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791182A>G , CM000667.2:g.90791182A>G	GRCh38
NC_000005.9:g.90086999A>G , CM000667.1:g.90086999A>G	GRCh37
NC_000005.8:g.90122755A>G	NCBI36
NG_007083.1:g.237383A>G
NG_007083.2:g.266839A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14353A>G MANE Select	NP_115495.3:p.Ile4785Val
ENST00000405460.9:c.14353A>G MANE Select	ENSP00000384582.2:p.Ile4785Val
NM_032119.3:c.14353A>G	NP_115495.3:p.Ile4785Val
NR_003149.1:n.14366A>G
NR_003149.2:n.14369A>G
ENST00000405460.6:c.14353A>G	ENSP00000384582.2:p.Ile4785Val
ENST00000425867.2:c.1336A>G	ENSP00000392618.2:p.Ile446Val
ENST00000425867.3:c.3307A>G	ENSP00000392618.3:p.Ile1103Val
ENST00000507314.1:n.28A>G
ENST00000507314.2:c.28A>G	ENSP00000491299.1:p.Ile10Val
ENST00000638510.1:n.1620A>G
ENST00000638585.1:n.119A>G
ENST00000638975.1:c.982A>G	ENSP00000492630.1:p.Ile328Val
ENST00000639431.1:c.265+114973A>G	ENSP00000491057.1:n.265+114973A>G
ENST00000640407.1:c.763A>G	ENSP00000491425.1:p.Ile255Val
XM_011543675.1:c.14350A>G	XP_011541977.1:p.Ile4784Val
XM_011543676.1:c.14272A>G	XP_011541978.1:p.Ile4758Val
XM_011543677.1:c.11656A>G	XP_011541979.1:p.Ile3886Val
XM_011543678.1:c.14353A>G	XP_011541980.1:p.Ile4785Val
XM_017009963.2:c.14374A>G	XP_016865452.1:p.Ile4792Val
XM_017009964.2:c.14371A>G	XP_016865453.1:p.Ile4791Val
XM_017009965.1:c.14371A>G	XP_016865454.1:p.Ile4791Val
XM_017009966.2:c.14293A>G	XP_016865455.1:p.Ile4765Val
XM_017009967.1:c.14278A>G	XP_016865456.1:p.Ile4760Val
XM_017009968.2:c.14374A>G	XP_016865457.1:p.Ile4792Val
XM_017009969.2:c.14374A>G	XP_016865458.1:p.Ile4792Val
XM_017009970.2:c.14374A>G	XP_016865459.1:p.Ile4792Val
XM_017009971.2:c.14374A>G	XP_016865460.1:p.Ile4792Val
XM_017009972.1:c.7492A>G	XP_016865461.1:p.Ile2498Val
XM_017009973.1:c.7471A>G	XP_016865462.1:p.Ile2491Val