Canonical Allele Identifier: CA2767405896

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716745_90716746insAG , CM000667.2:g.90716745_90716746insAG	GRCh38
NC_000005.9:g.90012562_90012563insAG , CM000667.1:g.90012562_90012563insAG	GRCh37
NC_000005.8:g.90048318_90048319insAG	NCBI36
NG_007083.1:g.162946_162947insAG
NG_007083.2:g.192402_192403insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9447+16_9447+17insAG MANE Select	ENSP00000384582.2:n.9447+16_9447+17insAG
ENST00000639431.1:c.265+40536_265+40537insAG	ENSP00000491057.1:n.265+40536_265+40537insAG
ENST00000639473.1:n.4922_4923insAG
ENST00000640374.1:n.2591+16_2591+17insAG
ENST00000640779.1:c.4176+16_4176+17insAG
ENST00000405460.6:c.9447+16_9447+17insAG	ENSP00000384582.2:n.9447+16_9447+17insAG
ENST00000509621.1:c.2144+16_2144+17insAG
NM_032119.3:c.9447+16_9447+17insAG	NP_115495.3:n.9447+16_9447+17insAG
NR_003149.1:n.9460+16_9460+17insAG
XM_011543675.1:c.9444+16_9444+17insAG	XP_011541977.1:n.9444+16_9444+17insAG
XM_011543676.1:c.9366+16_9366+17insAG	XP_011541978.1:n.9366+16_9366+17insAG
XM_011543677.1:c.6750+16_6750+17insAG	XP_011541979.1:n.6750+16_6750+17insAG
XM_011543678.1:c.9447+16_9447+17insAG	XP_011541980.1:n.9447+16_9447+17insAG
XM_011543679.1:c.9447+16_9447+17insAG	XP_011541981.1:n.9447+16_9447+17insAG
XR_948560.1:n.272-937_272-936insCT
NM_032119.4:c.9447+16_9447+17insAG MANE Select	NP_115495.3:n.9447+16_9447+17insAG
XM_017009963.2:c.9468+16_9468+17insAG	XP_016865452.1:n.9468+16_9468+17insAG
XM_017009964.2:c.9465+16_9465+17insAG	XP_016865453.1:n.9465+16_9465+17insAG
XM_017009965.1:c.9465+16_9465+17insAG	XP_016865454.1:n.9465+16_9465+17insAG
XM_017009966.2:c.9387+16_9387+17insAG	XP_016865455.1:n.9387+16_9387+17insAG
XM_017009967.1:c.9372+16_9372+17insAG	XP_016865456.1:n.9372+16_9372+17insAG
XM_017009968.2:c.9468+16_9468+17insAG	XP_016865457.1:n.9468+16_9468+17insAG
XM_017009969.2:c.9468+16_9468+17insAG	XP_016865458.1:n.9468+16_9468+17insAG
XM_017009970.2:c.9468+16_9468+17insAG	XP_016865459.1:n.9468+16_9468+17insAG
XM_017009971.2:c.9468+16_9468+17insAG	XP_016865460.1:n.9468+16_9468+17insAG
XM_017009972.1:c.2586+16_2586+17insAG	XP_016865461.1:n.2586+16_2586+17insAG
XM_017009973.1:c.2565+16_2565+17insAG	XP_016865462.1:n.2565+16_2565+17insAG
XM_017009974.2:c.9468+16_9468+17insAG	XP_016865463.1:n.9468+16_9468+17insAG
XR_001742802.1:n.2523-937_2523-936insCT
NR_003149.2:n.9463+16_9463+17insAG