Canonical Allele Identifier: CA2767420618

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692884_90692885insAGA , CM000667.2:g.90692884_90692885insAGA	GRCh38
NC_000005.9:g.89988701_89988702insAGA , CM000667.1:g.89988701_89988702insAGA	GRCh37
NC_000005.8:g.90024457_90024458insAGA	NCBI36
NG_007083.1:g.139085_139086insAGA
NG_007083.2:g.168541_168542insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7133+98_7133+99insAGA MANE Select	ENSP00000384582.2:n.7133+98_7133+99insAGA
ENST00000639431.1:c.265+16675_265+16676insAGA	ENSP00000491057.1:n.265+16675_265+16676insAGA
ENST00000639473.1:n.2592+98_2592+99insAGA
ENST00000640012.1:c.940+98_940+99insAGA
ENST00000640374.1:n.277+98_277+99insAGA
ENST00000640403.1:c.4424+98_4424+99insAGA	ENSP00000492531.1:n.4424+98_4424+99insAGA
ENST00000640779.1:c.1862+98_1862+99insAGA
ENST00000405460.6:c.7133+98_7133+99insAGA	ENSP00000384582.2:n.7133+98_7133+99insAGA
NM_032119.3:c.7133+98_7133+99insAGA	NP_115495.3:n.7133+98_7133+99insAGA
NR_003149.1:n.7146+98_7146+99insAGA
XM_011543675.1:c.7130+98_7130+99insAGA	XP_011541977.1:n.7130+98_7130+99insAGA
XM_011543676.1:c.7052+98_7052+99insAGA	XP_011541978.1:n.7052+98_7052+99insAGA
XM_011543677.1:c.4436+98_4436+99insAGA	XP_011541979.1:n.4436+98_4436+99insAGA
XM_011543678.1:c.7133+98_7133+99insAGA	XP_011541980.1:n.7133+98_7133+99insAGA
XM_011543679.1:c.7133+98_7133+99insAGA	XP_011541981.1:n.7133+98_7133+99insAGA
NM_032119.4:c.7133+98_7133+99insAGA MANE Select	NP_115495.3:n.7133+98_7133+99insAGA
XM_017009963.2:c.7133+98_7133+99insAGA	XP_016865452.1:n.7133+98_7133+99insAGA
XM_017009964.2:c.7130+98_7130+99insAGA	XP_016865453.1:n.7130+98_7130+99insAGA
XM_017009965.1:c.7130+98_7130+99insAGA	XP_016865454.1:n.7130+98_7130+99insAGA
XM_017009966.2:c.7052+98_7052+99insAGA	XP_016865455.1:n.7052+98_7052+99insAGA
XM_017009967.1:c.7037+98_7037+99insAGA	XP_016865456.1:n.7037+98_7037+99insAGA
XM_017009968.2:c.7133+98_7133+99insAGA	XP_016865457.1:n.7133+98_7133+99insAGA
XM_017009969.2:c.7133+98_7133+99insAGA	XP_016865458.1:n.7133+98_7133+99insAGA
XM_017009970.2:c.7133+98_7133+99insAGA	XP_016865459.1:n.7133+98_7133+99insAGA
XM_017009971.2:c.7133+98_7133+99insAGA	XP_016865460.1:n.7133+98_7133+99insAGA
XM_017009972.1:c.251+98_251+99insAGA	XP_016865461.1:n.251+98_251+99insAGA
XM_017009973.1:c.251+98_251+99insAGA	XP_016865462.1:n.251+98_251+99insAGA
XM_017009974.2:c.7133+98_7133+99insAGA	XP_016865463.1:n.7133+98_7133+99insAGA
NR_003149.2:n.7149+98_7149+99insAGA