Canonical Allele Identifier: CA3339285

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90653628A>G , CM000667.2:g.90653628A>G	GRCh38
NC_000005.9:g.89949445A>G , CM000667.1:g.89949445A>G	GRCh37
NC_000005.8:g.89985201A>G	NCBI36
NG_007083.1:g.99829A>G
NG_007083.2:g.129285A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.4054A>G MANE Select	NP_115495.3:p.Ile1352Val
ENST00000405460.9:c.4054A>G MANE Select	ENSP00000384582.2:p.Ile1352Val
NM_032119.3:c.4054A>G	NP_115495.3:p.Ile1352Val
NR_003149.1:n.4150A>G
NR_003149.2:n.4153A>G
ENST00000405460.6:c.4054A>G	ENSP00000384582.2:p.Ile1352Val
ENST00000504142.1:c.2819A>G
ENST00000504142.2:n.2820A>G
ENST00000639676.1:n.1652A>G
ENST00000640403.1:c.1345A>G	ENSP00000492531.1:p.Ile449Val
XM_011543675.1:c.4054A>G	XP_011541977.1:p.Ile1352Val
XM_011543676.1:c.4054A>G	XP_011541978.1:p.Ile1352Val
XM_011543677.1:c.1357A>G	XP_011541979.1:p.Ile453Val
XM_011543678.1:c.4054A>G	XP_011541980.1:p.Ile1352Val
XM_011543679.1:c.4054A>G	XP_011541981.1:p.Ile1352Val
XM_017009963.2:c.4054A>G	XP_016865452.1:p.Ile1352Val
XM_017009964.2:c.4054A>G	XP_016865453.1:p.Ile1352Val
XM_017009965.1:c.4051A>G	XP_016865454.1:p.Ile1351Val
XM_017009966.2:c.4054A>G	XP_016865455.1:p.Ile1352Val
XM_017009967.1:c.3958A>G	XP_016865456.1:p.Ile1320Val
XM_017009968.2:c.4054A>G	XP_016865457.1:p.Ile1352Val
XM_017009969.2:c.4054A>G	XP_016865458.1:p.Ile1352Val
XM_017009970.2:c.4054A>G	XP_016865459.1:p.Ile1352Val
XM_017009971.2:c.4054A>G	XP_016865460.1:p.Ile1352Val
XM_017009974.2:c.4054A>G	XP_016865463.1:p.Ile1352Val