Canonical Allele Identifier: CA3341721

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791234G>A , CM000667.2:g.90791234G>A	GRCh38
NC_000005.9:g.90087051G>A , CM000667.1:g.90087051G>A	GRCh37
NC_000005.8:g.90122807G>A	NCBI36
NG_007083.1:g.237435G>A
NG_007083.2:g.266891G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14405G>A MANE Select	NP_115495.3:p.Arg4802Gln
ENST00000405460.9:c.14405G>A MANE Select	ENSP00000384582.2:p.Arg4802Gln
NM_032119.3:c.14405G>A	NP_115495.3:p.Arg4802Gln
NR_003149.1:n.14418G>A
NR_003149.2:n.14421G>A
ENST00000405460.6:c.14405G>A	ENSP00000384582.2:p.Arg4802Gln
ENST00000425867.2:c.1388G>A	ENSP00000392618.2:p.Arg463Gln
ENST00000425867.3:c.3359G>A	ENSP00000392618.3:p.Arg1120Gln
ENST00000507314.1:n.80G>A
ENST00000507314.2:c.80G>A	ENSP00000491299.1:p.Arg27Gln
ENST00000638510.1:n.1672G>A
ENST00000638585.1:n.171G>A
ENST00000638975.1:c.1034G>A	ENSP00000492630.1:p.Arg345Gln
ENST00000639431.1:c.265+115025G>A	ENSP00000491057.1:n.265+115025G>A
ENST00000640407.1:c.815G>A	ENSP00000491425.1:p.Arg272Gln
XM_011543675.1:c.14402G>A	XP_011541977.1:p.Arg4801Gln
XM_011543676.1:c.14324G>A	XP_011541978.1:p.Arg4775Gln
XM_011543677.1:c.11708G>A	XP_011541979.1:p.Arg3903Gln
XM_011543678.1:c.14405G>A	XP_011541980.1:p.Arg4802Gln
XM_017009963.2:c.14426G>A	XP_016865452.1:p.Arg4809Gln
XM_017009964.2:c.14423G>A	XP_016865453.1:p.Arg4808Gln
XM_017009965.1:c.14423G>A	XP_016865454.1:p.Arg4808Gln
XM_017009966.2:c.14345G>A	XP_016865455.1:p.Arg4782Gln
XM_017009967.1:c.14330G>A	XP_016865456.1:p.Arg4777Gln
XM_017009968.2:c.14426G>A	XP_016865457.1:p.Arg4809Gln
XM_017009969.2:c.14426G>A	XP_016865458.1:p.Arg4809Gln
XM_017009970.2:c.14426G>A	XP_016865459.1:p.Arg4809Gln
XM_017009971.2:c.14426G>A	XP_016865460.1:p.Arg4809Gln
XM_017009972.1:c.7544G>A	XP_016865461.1:p.Arg2515Gln
XM_017009973.1:c.7523G>A	XP_016865462.1:p.Arg2508Gln