Canonical Allele Identifier: CA3341973

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810997G>A , CM000667.2:g.90810997G>A	GRCh38
NC_000005.9:g.90106814G>A , CM000667.1:g.90106814G>A	GRCh37
NC_000005.8:g.90142570G>A	NCBI36
NG_007083.1:g.257198G>A
NG_007083.2:g.286654G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15737G>A MANE Select	NP_115495.3:p.Arg5246Gln
ENST00000405460.9:c.15737G>A MANE Select	ENSP00000384582.2:p.Arg5246Gln
NM_032119.3:c.15737G>A	NP_115495.3:p.Arg5246Gln
NR_003149.1:n.15750G>A
NR_003149.2:n.15753G>A
ENST00000405460.6:c.15737G>A	ENSP00000384582.2:p.Arg5246Gln
ENST00000425867.2:c.2720G>A	ENSP00000392618.2:p.Arg907Gln
ENST00000425867.3:c.4691G>A	ENSP00000392618.3:p.Arg1564Gln
ENST00000638510.1:n.3004G>A
ENST00000639431.1:c.265+134788G>A	ENSP00000491057.1:n.265+134788G>A
ENST00000640407.1:c.2147G>A	ENSP00000491425.1:p.Arg716Gln
XM_011543675.1:c.15734G>A	XP_011541977.1:p.Arg5245Gln
XM_011543676.1:c.15656G>A	XP_011541978.1:p.Arg5219Gln
XM_011543677.1:c.13040G>A	XP_011541979.1:p.Arg4347Gln
XM_017009963.2:c.15758G>A	XP_016865452.1:p.Arg5253Gln
XM_017009964.2:c.15755G>A	XP_016865453.1:p.Arg5252Gln
XM_017009965.1:c.15755G>A	XP_016865454.1:p.Arg5252Gln
XM_017009966.2:c.15677G>A	XP_016865455.1:p.Arg5226Gln
XM_017009967.1:c.15662G>A	XP_016865456.1:p.Arg5221Gln
XM_017009968.2:c.15578G>A	XP_016865457.1:p.Arg5193Gln
XM_017009969.2:c.15758G>A	XP_016865458.1:p.Arg5253Gln
XM_017009972.1:c.8876G>A	XP_016865461.1:p.Arg2959Gln
XM_017009973.1:c.8855G>A	XP_016865462.1:p.Arg2952Gln