Canonical Allele Identifier: CA2767405942

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716766_90716767insACAG , CM000667.2:g.90716766_90716767insACAG	GRCh38
NC_000005.9:g.90012583_90012584insACAG , CM000667.1:g.90012583_90012584insACAG	GRCh37
NC_000005.8:g.90048339_90048340insACAG	NCBI36
NG_007083.1:g.162967_162968insACAG
NG_007083.2:g.192423_192424insACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9447+37_9447+38insACAG MANE Select	ENSP00000384582.2:n.9447+37_9447+38insACAG
ENST00000639431.1:c.265+40557_265+40558insACAG	ENSP00000491057.1:n.265+40557_265+40558insACAG
ENST00000639473.1:n.4943_4944insACAG
ENST00000640374.1:n.2591+37_2591+38insACAG
ENST00000640779.1:c.4176+37_4176+38insACAG
ENST00000405460.6:c.9447+37_9447+38insACAG	ENSP00000384582.2:n.9447+37_9447+38insACAG
ENST00000509621.1:c.2144+37_2144+38insACAG
NM_032119.3:c.9447+37_9447+38insACAG	NP_115495.3:n.9447+37_9447+38insACAG
NR_003149.1:n.9460+37_9460+38insACAG
XM_011543675.1:c.9444+37_9444+38insACAG	XP_011541977.1:n.9444+37_9444+38insACAG
XM_011543676.1:c.9366+37_9366+38insACAG	XP_011541978.1:n.9366+37_9366+38insACAG
XM_011543677.1:c.6750+37_6750+38insACAG	XP_011541979.1:n.6750+37_6750+38insACAG
XM_011543678.1:c.9447+37_9447+38insACAG	XP_011541980.1:n.9447+37_9447+38insACAG
XM_011543679.1:c.9447+37_9447+38insACAG	XP_011541981.1:n.9447+37_9447+38insACAG
XR_948560.1:n.272-958_272-957insCTGT
NM_032119.4:c.9447+37_9447+38insACAG MANE Select	NP_115495.3:n.9447+37_9447+38insACAG
XM_017009963.2:c.9468+37_9468+38insACAG	XP_016865452.1:n.9468+37_9468+38insACAG
XM_017009964.2:c.9465+37_9465+38insACAG	XP_016865453.1:n.9465+37_9465+38insACAG
XM_017009965.1:c.9465+37_9465+38insACAG	XP_016865454.1:n.9465+37_9465+38insACAG
XM_017009966.2:c.9387+37_9387+38insACAG	XP_016865455.1:n.9387+37_9387+38insACAG
XM_017009967.1:c.9372+37_9372+38insACAG	XP_016865456.1:n.9372+37_9372+38insACAG
XM_017009968.2:c.9468+37_9468+38insACAG	XP_016865457.1:n.9468+37_9468+38insACAG
XM_017009969.2:c.9468+37_9468+38insACAG	XP_016865458.1:n.9468+37_9468+38insACAG
XM_017009970.2:c.9468+37_9468+38insACAG	XP_016865459.1:n.9468+37_9468+38insACAG
XM_017009971.2:c.9468+37_9468+38insACAG	XP_016865460.1:n.9468+37_9468+38insACAG
XM_017009972.1:c.2586+37_2586+38insACAG	XP_016865461.1:n.2586+37_2586+38insACAG
XM_017009973.1:c.2565+37_2565+38insACAG	XP_016865462.1:n.2565+37_2565+38insACAG
XM_017009974.2:c.9468+37_9468+38insACAG	XP_016865463.1:n.9468+37_9468+38insACAG
XR_001742802.1:n.2523-958_2523-957insCTGT
NR_003149.2:n.9463+37_9463+38insACAG