Canonical Allele Identifier: CA2767405963

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716771_90716772insAG , CM000667.2:g.90716771_90716772insAG	GRCh38
NC_000005.9:g.90012588_90012589insAG , CM000667.1:g.90012588_90012589insAG	GRCh37
NC_000005.8:g.90048344_90048345insAG	NCBI36
NG_007083.1:g.162972_162973insAG
NG_007083.2:g.192428_192429insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9447+42_9447+43insAG MANE Select	ENSP00000384582.2:n.9447+42_9447+43insAG
ENST00000639431.1:c.265+40562_265+40563insAG	ENSP00000491057.1:n.265+40562_265+40563insAG
ENST00000639473.1:n.4948_4949insAG
ENST00000640374.1:n.2591+42_2591+43insAG
ENST00000640779.1:c.4176+42_4176+43insAG
ENST00000405460.6:c.9447+42_9447+43insAG	ENSP00000384582.2:n.9447+42_9447+43insAG
ENST00000509621.1:c.2144+42_2144+43insAG
NM_032119.3:c.9447+42_9447+43insAG	NP_115495.3:n.9447+42_9447+43insAG
NR_003149.1:n.9460+42_9460+43insAG
XM_011543675.1:c.9444+42_9444+43insAG	XP_011541977.1:n.9444+42_9444+43insAG
XM_011543676.1:c.9366+42_9366+43insAG	XP_011541978.1:n.9366+42_9366+43insAG
XM_011543677.1:c.6750+42_6750+43insAG	XP_011541979.1:n.6750+42_6750+43insAG
XM_011543678.1:c.9447+42_9447+43insAG	XP_011541980.1:n.9447+42_9447+43insAG
XM_011543679.1:c.9447+42_9447+43insAG	XP_011541981.1:n.9447+42_9447+43insAG
XR_948560.1:n.272-963_272-962insCT
NM_032119.4:c.9447+42_9447+43insAG MANE Select	NP_115495.3:n.9447+42_9447+43insAG
XM_017009963.2:c.9468+42_9468+43insAG	XP_016865452.1:n.9468+42_9468+43insAG
XM_017009964.2:c.9465+42_9465+43insAG	XP_016865453.1:n.9465+42_9465+43insAG
XM_017009965.1:c.9465+42_9465+43insAG	XP_016865454.1:n.9465+42_9465+43insAG
XM_017009966.2:c.9387+42_9387+43insAG	XP_016865455.1:n.9387+42_9387+43insAG
XM_017009967.1:c.9372+42_9372+43insAG	XP_016865456.1:n.9372+42_9372+43insAG
XM_017009968.2:c.9468+42_9468+43insAG	XP_016865457.1:n.9468+42_9468+43insAG
XM_017009969.2:c.9468+42_9468+43insAG	XP_016865458.1:n.9468+42_9468+43insAG
XM_017009970.2:c.9468+42_9468+43insAG	XP_016865459.1:n.9468+42_9468+43insAG
XM_017009971.2:c.9468+42_9468+43insAG	XP_016865460.1:n.9468+42_9468+43insAG
XM_017009972.1:c.2586+42_2586+43insAG	XP_016865461.1:n.2586+42_2586+43insAG
XM_017009973.1:c.2565+42_2565+43insAG	XP_016865462.1:n.2565+42_2565+43insAG
XM_017009974.2:c.9468+42_9468+43insAG	XP_016865463.1:n.9468+42_9468+43insAG
XR_001742802.1:n.2523-963_2523-962insCT
NR_003149.2:n.9463+42_9463+43insAG