Canonical Allele Identifier: CA10576666

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90706249A>G , CM000667.2:g.90706249A>G	GRCh38
NC_000005.9:g.90002066A>G , CM000667.1:g.90002066A>G	GRCh37
NC_000005.8:g.90037822A>G	NCBI36
NG_007083.1:g.152450A>G
NG_007083.2:g.181906A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8585A>G MANE Select	NP_115495.3:p.Tyr2862Cys
ENST00000405460.9:c.8585A>G MANE Select	ENSP00000384582.2:p.Tyr2862Cys
NM_032119.3:c.8585A>G	NP_115495.3:p.Tyr2862Cys
NR_003149.1:n.8598A>G
NR_003149.2:n.8601A>G
ENST00000405460.6:c.8585A>G	ENSP00000384582.2:p.Tyr2862Cys
ENST00000509621.1:c.1282A>G
ENST00000639431.1:c.265+30040A>G	ENSP00000491057.1:n.265+30040A>G
ENST00000639473.1:n.4044A>G
ENST00000640012.1:c.2392A>G
ENST00000640374.1:n.1729A>G
ENST00000640403.1:c.5876A>G	ENSP00000492531.1:p.Tyr1959Cys
ENST00000640779.1:c.3314A>G
XM_011543675.1:c.8582A>G	XP_011541977.1:p.Tyr2861Cys
XM_011543676.1:c.8504A>G	XP_011541978.1:p.Tyr2835Cys
XM_011543677.1:c.5888A>G	XP_011541979.1:p.Tyr1963Cys
XM_011543678.1:c.8585A>G	XP_011541980.1:p.Tyr2862Cys
XM_011543679.1:c.8585A>G	XP_011541981.1:p.Tyr2862Cys
XM_017009963.2:c.8606A>G	XP_016865452.1:p.Tyr2869Cys
XM_017009964.2:c.8603A>G	XP_016865453.1:p.Tyr2868Cys
XM_017009965.1:c.8603A>G	XP_016865454.1:p.Tyr2868Cys
XM_017009966.2:c.8525A>G	XP_016865455.1:p.Tyr2842Cys
XM_017009967.1:c.8510A>G	XP_016865456.1:p.Tyr2837Cys
XM_017009968.2:c.8606A>G	XP_016865457.1:p.Tyr2869Cys
XM_017009969.2:c.8606A>G	XP_016865458.1:p.Tyr2869Cys
XM_017009970.2:c.8606A>G	XP_016865459.1:p.Tyr2869Cys
XM_017009971.2:c.8606A>G	XP_016865460.1:p.Tyr2869Cys
XM_017009972.1:c.1724A>G	XP_016865461.1:p.Tyr575Cys
XM_017009973.1:c.1703A>G	XP_016865462.1:p.Tyr568Cys
XM_017009974.2:c.8606A>G	XP_016865463.1:p.Tyr2869Cys