Canonical Allele Identifier: CA2767420604

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692864_90692865insG , CM000667.2:g.90692864_90692865insG	GRCh38
NC_000005.9:g.89988681_89988682insG , CM000667.1:g.89988681_89988682insG	GRCh37
NC_000005.8:g.90024437_90024438insG	NCBI36
NG_007083.1:g.139065_139066insG
NG_007083.2:g.168521_168522insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7133+78_7133+79insG MANE Select	ENSP00000384582.2:n.7133+78_7133+79insG
ENST00000639431.1:c.265+16655_265+16656insG	ENSP00000491057.1:n.265+16655_265+16656insG
ENST00000639473.1:n.2592+78_2592+79insG
ENST00000640012.1:c.940+78_940+79insG
ENST00000640374.1:n.277+78_277+79insG
ENST00000640403.1:c.4424+78_4424+79insG	ENSP00000492531.1:n.4424+78_4424+79insG
ENST00000640779.1:c.1862+78_1862+79insG
ENST00000405460.6:c.7133+78_7133+79insG	ENSP00000384582.2:n.7133+78_7133+79insG
NM_032119.3:c.7133+78_7133+79insG	NP_115495.3:n.7133+78_7133+79insG
NR_003149.1:n.7146+78_7146+79insG
XM_011543675.1:c.7130+78_7130+79insG	XP_011541977.1:n.7130+78_7130+79insG
XM_011543676.1:c.7052+78_7052+79insG	XP_011541978.1:n.7052+78_7052+79insG
XM_011543677.1:c.4436+78_4436+79insG	XP_011541979.1:n.4436+78_4436+79insG
XM_011543678.1:c.7133+78_7133+79insG	XP_011541980.1:n.7133+78_7133+79insG
XM_011543679.1:c.7133+78_7133+79insG	XP_011541981.1:n.7133+78_7133+79insG
NM_032119.4:c.7133+78_7133+79insG MANE Select	NP_115495.3:n.7133+78_7133+79insG
XM_017009963.2:c.7133+78_7133+79insG	XP_016865452.1:n.7133+78_7133+79insG
XM_017009964.2:c.7130+78_7130+79insG	XP_016865453.1:n.7130+78_7130+79insG
XM_017009965.1:c.7130+78_7130+79insG	XP_016865454.1:n.7130+78_7130+79insG
XM_017009966.2:c.7052+78_7052+79insG	XP_016865455.1:n.7052+78_7052+79insG
XM_017009967.1:c.7037+78_7037+79insG	XP_016865456.1:n.7037+78_7037+79insG
XM_017009968.2:c.7133+78_7133+79insG	XP_016865457.1:n.7133+78_7133+79insG
XM_017009969.2:c.7133+78_7133+79insG	XP_016865458.1:n.7133+78_7133+79insG
XM_017009970.2:c.7133+78_7133+79insG	XP_016865459.1:n.7133+78_7133+79insG
XM_017009971.2:c.7133+78_7133+79insG	XP_016865460.1:n.7133+78_7133+79insG
XM_017009972.1:c.251+78_251+79insG	XP_016865461.1:n.251+78_251+79insG
XM_017009973.1:c.251+78_251+79insG	XP_016865462.1:n.251+78_251+79insG
XM_017009974.2:c.7133+78_7133+79insG	XP_016865463.1:n.7133+78_7133+79insG
NR_003149.2:n.7149+78_7149+79insG