Canonical Allele Identifier: CA3342559

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985495A>G , CM000667.2:g.90985495A>G	GRCh38
NC_000005.9:g.90281312A>G , CM000667.1:g.90281312A>G	GRCh37
NC_000005.8:g.90317068A>G	NCBI36
NG_007083.1:g.431696A>G
NG_007083.2:g.461152A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18125A>G MANE Select	NP_115495.3:p.Gln6042Arg
ENST00000405460.9:c.18125A>G MANE Select	ENSP00000384582.2:p.Gln6042Arg
NM_032119.3:c.18125A>G	NP_115495.3:p.Gln6042Arg
NR_003149.1:n.18138A>G
NR_003149.2:n.18141A>G
ENST00000405460.6:c.18125A>G	ENSP00000384582.2:p.Gln6042Arg
ENST00000425867.2:c.5108A>G	ENSP00000392618.2:p.Gln1703Arg
ENST00000425867.3:c.7079A>G	ENSP00000392618.3:p.Gln2360Arg
ENST00000638510.1:n.5392A>G
ENST00000638990.1:c.1337A>G
ENST00000639431.1:c.417A>G	ENSP00000491057.1:n.417A>G
ENST00000639707.1:c.209A>G	ENSP00000492328.1:p.Gln70Arg
ENST00000639821.1:c.209A>G	ENSP00000492216.1:p.Gln70Arg
ENST00000640369.1:c.209A>G	ENSP00000491401.1:p.Gln70Arg
ENST00000640407.1:c.4574A>G	ENSP00000491425.1:n.4574A>G
ENST00000640815.1:c.209A>G	ENSP00000491767.1:p.Gln70Arg
XM_011543675.1:c.18122A>G	XP_011541977.1:p.Gln6041Arg
XM_011543676.1:c.18044A>G	XP_011541978.1:p.Gln6015Arg
XM_011543677.1:c.15428A>G	XP_011541979.1:p.Gln5143Arg
XM_017009963.2:c.18146A>G	XP_016865452.1:p.Gln6049Arg
XM_017009964.2:c.18143A>G	XP_016865453.1:p.Gln6048Arg
XM_017009965.1:c.18143A>G	XP_016865454.1:p.Gln6048Arg
XM_017009966.2:c.18065A>G	XP_016865455.1:p.Gln6022Arg
XM_017009967.1:c.18050A>G	XP_016865456.1:p.Gln6017Arg
XM_017009968.2:c.17966A>G	XP_016865457.1:p.Gln5989Arg
XM_017009969.2:c.18146A>G	XP_016865458.1:p.Gln6049Arg
XM_017009972.1:c.11264A>G	XP_016865461.1:p.Gln3755Arg
XM_017009973.1:c.11243A>G	XP_016865462.1:p.Gln3748Arg