Canonical Allele Identifier: CA3342144

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90828944G>A , CM000667.2:g.90828944G>A	GRCh38
NC_000005.9:g.90124761G>A , CM000667.1:g.90124761G>A	GRCh37
NC_000005.8:g.90160517G>A	NCBI36
NG_007083.1:g.275145G>A
NG_007083.2:g.304601G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16369G>A MANE Select	NP_115495.3:p.Val5457Ile
ENST00000405460.9:c.16369G>A MANE Select	ENSP00000384582.2:p.Val5457Ile
NM_032119.3:c.16369G>A	NP_115495.3:p.Val5457Ile
NR_003149.1:n.16382G>A
NR_003149.2:n.16385G>A
ENST00000405460.6:c.16369G>A	ENSP00000384582.2:p.Val5457Ile
ENST00000425867.2:c.3352G>A	ENSP00000392618.2:p.Val1118Ile
ENST00000425867.3:c.5323G>A	ENSP00000392618.3:p.Val1775Ile
ENST00000638510.1:n.3636G>A
ENST00000639431.1:c.265+152735G>A	ENSP00000491057.1:n.265+152735G>A
ENST00000640061.1:n.128+6762G>A
ENST00000640407.1:c.2818G>A	ENSP00000491425.1:n.2818G>A
XM_011543675.1:c.16366G>A	XP_011541977.1:p.Val5456Ile
XM_011543676.1:c.16288G>A	XP_011541978.1:p.Val5430Ile
XM_011543677.1:c.13672G>A	XP_011541979.1:p.Val4558Ile
XM_017009963.2:c.16390G>A	XP_016865452.1:p.Val5464Ile
XM_017009964.2:c.16387G>A	XP_016865453.1:p.Val5463Ile
XM_017009965.1:c.16387G>A	XP_016865454.1:p.Val5463Ile
XM_017009966.2:c.16309G>A	XP_016865455.1:p.Val5437Ile
XM_017009967.1:c.16294G>A	XP_016865456.1:p.Val5432Ile
XM_017009968.2:c.16210G>A	XP_016865457.1:p.Val5404Ile
XM_017009969.2:c.16390G>A	XP_016865458.1:p.Val5464Ile
XM_017009972.1:c.9508G>A	XP_016865461.1:p.Val3170Ile
XM_017009973.1:c.9487G>A	XP_016865462.1:p.Val3163Ile