Canonical Allele Identifier: CA2767405921

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716761_90716762insAG , CM000667.2:g.90716761_90716762insAG	GRCh38
NC_000005.9:g.90012578_90012579insAG , CM000667.1:g.90012578_90012579insAG	GRCh37
NC_000005.8:g.90048334_90048335insAG	NCBI36
NG_007083.1:g.162962_162963insAG
NG_007083.2:g.192418_192419insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9447+32_9447+33insAG MANE Select	ENSP00000384582.2:n.9447+32_9447+33insAG
ENST00000639431.1:c.265+40552_265+40553insAG	ENSP00000491057.1:n.265+40552_265+40553insAG
ENST00000639473.1:n.4938_4939insAG
ENST00000640374.1:n.2591+32_2591+33insAG
ENST00000640779.1:c.4176+32_4176+33insAG
ENST00000405460.6:c.9447+32_9447+33insAG	ENSP00000384582.2:n.9447+32_9447+33insAG
ENST00000509621.1:c.2144+32_2144+33insAG
NM_032119.3:c.9447+32_9447+33insAG	NP_115495.3:n.9447+32_9447+33insAG
NR_003149.1:n.9460+32_9460+33insAG
XM_011543675.1:c.9444+32_9444+33insAG	XP_011541977.1:n.9444+32_9444+33insAG
XM_011543676.1:c.9366+32_9366+33insAG	XP_011541978.1:n.9366+32_9366+33insAG
XM_011543677.1:c.6750+32_6750+33insAG	XP_011541979.1:n.6750+32_6750+33insAG
XM_011543678.1:c.9447+32_9447+33insAG	XP_011541980.1:n.9447+32_9447+33insAG
XM_011543679.1:c.9447+32_9447+33insAG	XP_011541981.1:n.9447+32_9447+33insAG
XR_948560.1:n.272-953_272-952insCT
NM_032119.4:c.9447+32_9447+33insAG MANE Select	NP_115495.3:n.9447+32_9447+33insAG
XM_017009963.2:c.9468+32_9468+33insAG	XP_016865452.1:n.9468+32_9468+33insAG
XM_017009964.2:c.9465+32_9465+33insAG	XP_016865453.1:n.9465+32_9465+33insAG
XM_017009965.1:c.9465+32_9465+33insAG	XP_016865454.1:n.9465+32_9465+33insAG
XM_017009966.2:c.9387+32_9387+33insAG	XP_016865455.1:n.9387+32_9387+33insAG
XM_017009967.1:c.9372+32_9372+33insAG	XP_016865456.1:n.9372+32_9372+33insAG
XM_017009968.2:c.9468+32_9468+33insAG	XP_016865457.1:n.9468+32_9468+33insAG
XM_017009969.2:c.9468+32_9468+33insAG	XP_016865458.1:n.9468+32_9468+33insAG
XM_017009970.2:c.9468+32_9468+33insAG	XP_016865459.1:n.9468+32_9468+33insAG
XM_017009971.2:c.9468+32_9468+33insAG	XP_016865460.1:n.9468+32_9468+33insAG
XM_017009972.1:c.2586+32_2586+33insAG	XP_016865461.1:n.2586+32_2586+33insAG
XM_017009973.1:c.2565+32_2565+33insAG	XP_016865462.1:n.2565+32_2565+33insAG
XM_017009974.2:c.9468+32_9468+33insAG	XP_016865463.1:n.9468+32_9468+33insAG
XR_001742802.1:n.2523-953_2523-952insCT
NR_003149.2:n.9463+32_9463+33insAG