Canonical Allele Identifier: CA138269

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720066A>G , CM000667.2:g.90720066A>G	GRCh38
NC_000005.9:g.90015883A>G , CM000667.1:g.90015883A>G	GRCh37
NC_000005.8:g.90051639A>G	NCBI36
NG_007083.1:g.166267A>G
NG_007083.2:g.195723A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9466A>G MANE Select	NP_115495.3:p.Ile3156Val
ENST00000405460.9:c.9466A>G MANE Select	ENSP00000384582.2:p.Ile3156Val
NM_032119.3:c.9466A>G	NP_115495.3:p.Ile3156Val
NR_003149.1:n.9479A>G
NR_003149.2:n.9482A>G
ENST00000405460.6:c.9466A>G	ENSP00000384582.2:p.Ile3156Val
ENST00000509621.1:c.2163A>G
ENST00000639431.1:c.265+43857A>G	ENSP00000491057.1:n.265+43857A>G
ENST00000640374.1:n.2610A>G
ENST00000640779.1:c.4195A>G
XM_011543675.1:c.9463A>G	XP_011541977.1:p.Ile3155Val
XM_011543676.1:c.9385A>G	XP_011541978.1:p.Ile3129Val
XM_011543677.1:c.6769A>G	XP_011541979.1:p.Ile2257Val
XM_011543678.1:c.9466A>G	XP_011541980.1:p.Ile3156Val
XM_011543679.1:c.9466A>G	XP_011541981.1:p.Ile3156Val
XM_017009963.2:c.9487A>G	XP_016865452.1:p.Ile3163Val
XM_017009964.2:c.9484A>G	XP_016865453.1:p.Ile3162Val
XM_017009965.1:c.9484A>G	XP_016865454.1:p.Ile3162Val
XM_017009966.2:c.9406A>G	XP_016865455.1:p.Ile3136Val
XM_017009967.1:c.9391A>G	XP_016865456.1:p.Ile3131Val
XM_017009968.2:c.9487A>G	XP_016865457.1:p.Ile3163Val
XM_017009969.2:c.9487A>G	XP_016865458.1:p.Ile3163Val
XM_017009970.2:c.9487A>G	XP_016865459.1:p.Ile3163Val
XM_017009971.2:c.9487A>G	XP_016865460.1:p.Ile3163Val
XM_017009972.1:c.2605A>G	XP_016865461.1:p.Ile869Val
XM_017009973.1:c.2584A>G	XP_016865462.1:p.Ile862Val
XM_017009974.2:c.9487A>G	XP_016865463.1:p.Ile3163Val
XR_001742802.1:n.2523-4257T>C
XR_948560.1:n.272-4257T>C