Canonical Allele Identifier: CA3342355

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90853467G>A , CM000667.2:g.90853467G>A	GRCh38
NC_000005.9:g.90149284G>A , CM000667.1:g.90149284G>A	GRCh37
NC_000005.8:g.90185040G>A	NCBI36
NG_007083.1:g.299668G>A
NG_007083.2:g.329124G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17388G>A MANE Select	NP_115495.3:p.Gln5796=
ENST00000405460.9:c.17388G>A MANE Select	ENSP00000384582.2:p.Gln5796=
NM_032119.3:c.17388G>A	NP_115495.3:p.Gln5796=
NR_003149.1:n.17401G>A
NR_003149.2:n.17404G>A
ENST00000405460.6:c.17388G>A	ENSP00000384582.2:p.Gln5796=
ENST00000425867.2:c.4371G>A	ENSP00000392618.2:p.Gln1457=
ENST00000425867.3:c.6342G>A	ENSP00000392618.3:p.Gln2114=
ENST00000638510.1:n.4655G>A
ENST00000638990.1:c.600G>A
ENST00000639431.1:c.266-131877G>A	ENSP00000491057.1:n.266-131877G>A
ENST00000640407.1:c.3837G>A	ENSP00000491425.1:n.3837G>A
XM_011543675.1:c.17385G>A	XP_011541977.1:p.Gln5795=
XM_011543676.1:c.17307G>A	XP_011541978.1:p.Gln5769=
XM_011543677.1:c.14691G>A	XP_011541979.1:p.Gln4897=
XM_017009963.2:c.17409G>A	XP_016865452.1:p.Gln5803=
XM_017009964.2:c.17406G>A	XP_016865453.1:p.Gln5802=
XM_017009965.1:c.17406G>A	XP_016865454.1:p.Gln5802=
XM_017009966.2:c.17328G>A	XP_016865455.1:p.Gln5776=
XM_017009967.1:c.17313G>A	XP_016865456.1:p.Gln5771=
XM_017009968.2:c.17229G>A	XP_016865457.1:p.Gln5743=
XM_017009969.2:c.17409G>A	XP_016865458.1:p.Gln5803=
XM_017009972.1:c.10527G>A	XP_016865461.1:p.Gln3509=
XM_017009973.1:c.10506G>A	XP_016865462.1:p.Gln3502=