Canonical Allele Identifier: CA2767405983

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716781_90716782insCAAAACCCAAACACACCCAACAC , CM000667.2:g.90716781_90716782insCAAAACCCAAACACACCCAACAC	GRCh38
NC_000005.9:g.90012598_90012599insCAAAACCCAAACACACCCAACAC , CM000667.1:g.90012598_90012599insCAAAACCCAAACACACCCAACAC	GRCh37
NC_000005.8:g.90048354_90048355insCAAAACCCAAACACACCCAACAC	NCBI36
NG_007083.1:g.162982_162983insCAAAACCCAAACACACCCAACAC
NG_007083.2:g.192438_192439insCAAAACCCAAACACACCCAACAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9447+52_9447+53insCAAAACCCAAACACACCCAACAC MANE Select	ENSP00000384582.2:n.9447+52_9447+53insCAAAACCCAAACACACCCAACAC...
ENST00000639431.1:c.265+40572_265+40573insCAAAACCCAAACACACCCAACAC	ENSP00000491057.1:n.265+40572_265+40573insCAAAACCCAAACACACCCA...
ENST00000639473.1:n.4958_4959insCAAAACCCAAACACACCCAACAC
ENST00000640374.1:n.2591+52_2591+53insCAAAACCCAAACACACCCAACAC
ENST00000640779.1:c.4176+52_4176+53insCAAAACCCAAACACACCCAACAC
ENST00000405460.6:c.9447+52_9447+53insCAAAACCCAAACACACCCAACAC	ENSP00000384582.2:n.9447+52_9447+53insCAAAACCCAAACACACCCAACAC...
ENST00000509621.1:c.2144+52_2144+53insCAAAACCCAAACACACCCAACAC
NM_032119.3:c.9447+52_9447+53insCAAAACCCAAACACACCCAACAC	NP_115495.3:n.9447+52_9447+53insCAAAACCCAAACACACCCAACAC
NR_003149.1:n.9460+52_9460+53insCAAAACCCAAACACACCCAACAC
XM_011543675.1:c.9444+52_9444+53insCAAAACCCAAACACACCCAACAC	XP_011541977.1:n.9444+52_9444+53insCAAAACCCAAACACACCCAACAC
XM_011543676.1:c.9366+52_9366+53insCAAAACCCAAACACACCCAACAC	XP_011541978.1:n.9366+52_9366+53insCAAAACCCAAACACACCCAACAC
XM_011543677.1:c.6750+52_6750+53insCAAAACCCAAACACACCCAACAC	XP_011541979.1:n.6750+52_6750+53insCAAAACCCAAACACACCCAACAC
XM_011543678.1:c.9447+52_9447+53insCAAAACCCAAACACACCCAACAC	XP_011541980.1:n.9447+52_9447+53insCAAAACCCAAACACACCCAACAC
XM_011543679.1:c.9447+52_9447+53insCAAAACCCAAACACACCCAACAC	XP_011541981.1:n.9447+52_9447+53insCAAAACCCAAACACACCCAACAC
XR_948560.1:n.272-973_272-972insGTGTTGGGTGTGTTTGGGTTTTG
NM_032119.4:c.9447+52_9447+53insCAAAACCCAAACACACCCAACAC MANE Select	NP_115495.3:n.9447+52_9447+53insCAAAACCCAAACACACCCAACAC
XM_017009963.2:c.9468+52_9468+53insCAAAACCCAAACACACCCAACAC	XP_016865452.1:n.9468+52_9468+53insCAAAACCCAAACACACCCAACAC
XM_017009964.2:c.9465+52_9465+53insCAAAACCCAAACACACCCAACAC	XP_016865453.1:n.9465+52_9465+53insCAAAACCCAAACACACCCAACAC
XM_017009965.1:c.9465+52_9465+53insCAAAACCCAAACACACCCAACAC	XP_016865454.1:n.9465+52_9465+53insCAAAACCCAAACACACCCAACAC
XM_017009966.2:c.9387+52_9387+53insCAAAACCCAAACACACCCAACAC	XP_016865455.1:n.9387+52_9387+53insCAAAACCCAAACACACCCAACAC
XM_017009967.1:c.9372+52_9372+53insCAAAACCCAAACACACCCAACAC	XP_016865456.1:n.9372+52_9372+53insCAAAACCCAAACACACCCAACAC
XM_017009968.2:c.9468+52_9468+53insCAAAACCCAAACACACCCAACAC	XP_016865457.1:n.9468+52_9468+53insCAAAACCCAAACACACCCAACAC
XM_017009969.2:c.9468+52_9468+53insCAAAACCCAAACACACCCAACAC	XP_016865458.1:n.9468+52_9468+53insCAAAACCCAAACACACCCAACAC
XM_017009970.2:c.9468+52_9468+53insCAAAACCCAAACACACCCAACAC	XP_016865459.1:n.9468+52_9468+53insCAAAACCCAAACACACCCAACAC
XM_017009971.2:c.9468+52_9468+53insCAAAACCCAAACACACCCAACAC	XP_016865460.1:n.9468+52_9468+53insCAAAACCCAAACACACCCAACAC
XM_017009972.1:c.2586+52_2586+53insCAAAACCCAAACACACCCAACAC	XP_016865461.1:n.2586+52_2586+53insCAAAACCCAAACACACCCAACAC
XM_017009973.1:c.2565+52_2565+53insCAAAACCCAAACACACCCAACAC	XP_016865462.1:n.2565+52_2565+53insCAAAACCCAAACACACCCAACAC
XM_017009974.2:c.9468+52_9468+53insCAAAACCCAAACACACCCAACAC	XP_016865463.1:n.9468+52_9468+53insCAAAACCCAAACACACCCAACAC
XR_001742802.1:n.2523-973_2523-972insGTGTTGGGTGTGTTTGGGTTTTG
NR_003149.2:n.9463+52_9463+53insCAAAACCCAAACACACCCAACAC