Canonical Allele Identifier: CA2767405936

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716765_90716766insAGAG , CM000667.2:g.90716765_90716766insAGAG	GRCh38
NC_000005.9:g.90012582_90012583insAGAG , CM000667.1:g.90012582_90012583insAGAG	GRCh37
NC_000005.8:g.90048338_90048339insAGAG	NCBI36
NG_007083.1:g.162966_162967insAGAG
NG_007083.2:g.192422_192423insAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9447+36_9447+37insAGAG MANE Select	ENSP00000384582.2:n.9447+36_9447+37insAGAG
ENST00000639431.1:c.265+40556_265+40557insAGAG	ENSP00000491057.1:n.265+40556_265+40557insAGAG
ENST00000639473.1:n.4942_4943insAGAG
ENST00000640374.1:n.2591+36_2591+37insAGAG
ENST00000640779.1:c.4176+36_4176+37insAGAG
ENST00000405460.6:c.9447+36_9447+37insAGAG	ENSP00000384582.2:n.9447+36_9447+37insAGAG
ENST00000509621.1:c.2144+36_2144+37insAGAG
NM_032119.3:c.9447+36_9447+37insAGAG	NP_115495.3:n.9447+36_9447+37insAGAG
NR_003149.1:n.9460+36_9460+37insAGAG
XM_011543675.1:c.9444+36_9444+37insAGAG	XP_011541977.1:n.9444+36_9444+37insAGAG
XM_011543676.1:c.9366+36_9366+37insAGAG	XP_011541978.1:n.9366+36_9366+37insAGAG
XM_011543677.1:c.6750+36_6750+37insAGAG	XP_011541979.1:n.6750+36_6750+37insAGAG
XM_011543678.1:c.9447+36_9447+37insAGAG	XP_011541980.1:n.9447+36_9447+37insAGAG
XM_011543679.1:c.9447+36_9447+37insAGAG	XP_011541981.1:n.9447+36_9447+37insAGAG
XR_948560.1:n.272-957_272-956insCTCT
NM_032119.4:c.9447+36_9447+37insAGAG MANE Select	NP_115495.3:n.9447+36_9447+37insAGAG
XM_017009963.2:c.9468+36_9468+37insAGAG	XP_016865452.1:n.9468+36_9468+37insAGAG
XM_017009964.2:c.9465+36_9465+37insAGAG	XP_016865453.1:n.9465+36_9465+37insAGAG
XM_017009965.1:c.9465+36_9465+37insAGAG	XP_016865454.1:n.9465+36_9465+37insAGAG
XM_017009966.2:c.9387+36_9387+37insAGAG	XP_016865455.1:n.9387+36_9387+37insAGAG
XM_017009967.1:c.9372+36_9372+37insAGAG	XP_016865456.1:n.9372+36_9372+37insAGAG
XM_017009968.2:c.9468+36_9468+37insAGAG	XP_016865457.1:n.9468+36_9468+37insAGAG
XM_017009969.2:c.9468+36_9468+37insAGAG	XP_016865458.1:n.9468+36_9468+37insAGAG
XM_017009970.2:c.9468+36_9468+37insAGAG	XP_016865459.1:n.9468+36_9468+37insAGAG
XM_017009971.2:c.9468+36_9468+37insAGAG	XP_016865460.1:n.9468+36_9468+37insAGAG
XM_017009972.1:c.2586+36_2586+37insAGAG	XP_016865461.1:n.2586+36_2586+37insAGAG
XM_017009973.1:c.2565+36_2565+37insAGAG	XP_016865462.1:n.2565+36_2565+37insAGAG
XM_017009974.2:c.9468+36_9468+37insAGAG	XP_016865463.1:n.9468+36_9468+37insAGAG
XR_001742802.1:n.2523-957_2523-956insCTCT
NR_003149.2:n.9463+36_9463+37insAGAG