Canonical Allele Identifier: CA2767405969

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716775_90716776insAGAC , CM000667.2:g.90716775_90716776insAGAC	GRCh38
NC_000005.9:g.90012592_90012593insAGAC , CM000667.1:g.90012592_90012593insAGAC	GRCh37
NC_000005.8:g.90048348_90048349insAGAC	NCBI36
NG_007083.1:g.162976_162977insAGAC
NG_007083.2:g.192432_192433insAGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9447+46_9447+47insAGAC MANE Select	ENSP00000384582.2:n.9447+46_9447+47insAGAC
ENST00000639431.1:c.265+40566_265+40567insAGAC	ENSP00000491057.1:n.265+40566_265+40567insAGAC
ENST00000639473.1:n.4952_4953insAGAC
ENST00000640374.1:n.2591+46_2591+47insAGAC
ENST00000640779.1:c.4176+46_4176+47insAGAC
ENST00000405460.6:c.9447+46_9447+47insAGAC	ENSP00000384582.2:n.9447+46_9447+47insAGAC
ENST00000509621.1:c.2144+46_2144+47insAGAC
NM_032119.3:c.9447+46_9447+47insAGAC	NP_115495.3:n.9447+46_9447+47insAGAC
NR_003149.1:n.9460+46_9460+47insAGAC
XM_011543675.1:c.9444+46_9444+47insAGAC	XP_011541977.1:n.9444+46_9444+47insAGAC
XM_011543676.1:c.9366+46_9366+47insAGAC	XP_011541978.1:n.9366+46_9366+47insAGAC
XM_011543677.1:c.6750+46_6750+47insAGAC	XP_011541979.1:n.6750+46_6750+47insAGAC
XM_011543678.1:c.9447+46_9447+47insAGAC	XP_011541980.1:n.9447+46_9447+47insAGAC
XM_011543679.1:c.9447+46_9447+47insAGAC	XP_011541981.1:n.9447+46_9447+47insAGAC
XR_948560.1:n.272-967_272-966insGTCT
NM_032119.4:c.9447+46_9447+47insAGAC MANE Select	NP_115495.3:n.9447+46_9447+47insAGAC
XM_017009963.2:c.9468+46_9468+47insAGAC	XP_016865452.1:n.9468+46_9468+47insAGAC
XM_017009964.2:c.9465+46_9465+47insAGAC	XP_016865453.1:n.9465+46_9465+47insAGAC
XM_017009965.1:c.9465+46_9465+47insAGAC	XP_016865454.1:n.9465+46_9465+47insAGAC
XM_017009966.2:c.9387+46_9387+47insAGAC	XP_016865455.1:n.9387+46_9387+47insAGAC
XM_017009967.1:c.9372+46_9372+47insAGAC	XP_016865456.1:n.9372+46_9372+47insAGAC
XM_017009968.2:c.9468+46_9468+47insAGAC	XP_016865457.1:n.9468+46_9468+47insAGAC
XM_017009969.2:c.9468+46_9468+47insAGAC	XP_016865458.1:n.9468+46_9468+47insAGAC
XM_017009970.2:c.9468+46_9468+47insAGAC	XP_016865459.1:n.9468+46_9468+47insAGAC
XM_017009971.2:c.9468+46_9468+47insAGAC	XP_016865460.1:n.9468+46_9468+47insAGAC
XM_017009972.1:c.2586+46_2586+47insAGAC	XP_016865461.1:n.2586+46_2586+47insAGAC
XM_017009973.1:c.2565+46_2565+47insAGAC	XP_016865462.1:n.2565+46_2565+47insAGAC
XM_017009974.2:c.9468+46_9468+47insAGAC	XP_016865463.1:n.9468+46_9468+47insAGAC
XR_001742802.1:n.2523-967_2523-966insGTCT
NR_003149.2:n.9463+46_9463+47insAGAC