Canonical Allele Identifier: CA3339413

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90672567A>G , CM000667.2:g.90672567A>G	GRCh38
NC_000005.9:g.89968384A>G , CM000667.1:g.89968384A>G	GRCh37
NC_000005.8:g.90004140A>G	NCBI36
NG_007083.1:g.118768A>G
NG_007083.2:g.148224A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.4774A>G MANE Select	NP_115495.3:p.Ile1592Val
ENST00000405460.9:c.4774A>G MANE Select	ENSP00000384582.2:p.Ile1592Val
NM_032119.3:c.4774A>G	NP_115495.3:p.Ile1592Val
NR_003149.1:n.4870A>G
NR_003149.2:n.4873A>G
ENST00000405460.6:c.4774A>G	ENSP00000384582.2:p.Ile1592Val
ENST00000450321.2:n.14A>G
ENST00000639473.1:n.233A>G
ENST00000639676.1:n.2372A>G
ENST00000640403.1:c.2065A>G	ENSP00000492531.1:p.Ile689Val
XM_011543675.1:c.4774A>G	XP_011541977.1:p.Ile1592Val
XM_011543676.1:c.4774A>G	XP_011541978.1:p.Ile1592Val
XM_011543677.1:c.2077A>G	XP_011541979.1:p.Ile693Val
XM_011543678.1:c.4774A>G	XP_011541980.1:p.Ile1592Val
XM_011543679.1:c.4774A>G	XP_011541981.1:p.Ile1592Val
XM_017009963.2:c.4774A>G	XP_016865452.1:p.Ile1592Val
XM_017009964.2:c.4774A>G	XP_016865453.1:p.Ile1592Val
XM_017009965.1:c.4771A>G	XP_016865454.1:p.Ile1591Val
XM_017009966.2:c.4774A>G	XP_016865455.1:p.Ile1592Val
XM_017009967.1:c.4678A>G	XP_016865456.1:p.Ile1560Val
XM_017009968.2:c.4774A>G	XP_016865457.1:p.Ile1592Val
XM_017009969.2:c.4774A>G	XP_016865458.1:p.Ile1592Val
XM_017009970.2:c.4774A>G	XP_016865459.1:p.Ile1592Val
XM_017009971.2:c.4774A>G	XP_016865460.1:p.Ile1592Val
XM_017009974.2:c.4774A>G	XP_016865463.1:p.Ile1592Val