Canonical Allele Identifier: CA2767420566

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692834_90692835insAGA , CM000667.2:g.90692834_90692835insAGA	GRCh38
NC_000005.9:g.89988651_89988652insAGA , CM000667.1:g.89988651_89988652insAGA	GRCh37
NC_000005.8:g.90024407_90024408insAGA	NCBI36
NG_007083.1:g.139035_139036insAGA
NG_007083.2:g.168491_168492insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7133+48_7133+49insAGA MANE Select	ENSP00000384582.2:n.7133+48_7133+49insAGA
ENST00000639431.1:c.265+16625_265+16626insAGA	ENSP00000491057.1:n.265+16625_265+16626insAGA
ENST00000639473.1:n.2592+48_2592+49insAGA
ENST00000640012.1:c.940+48_940+49insAGA
ENST00000640374.1:n.277+48_277+49insAGA
ENST00000640403.1:c.4424+48_4424+49insAGA	ENSP00000492531.1:n.4424+48_4424+49insAGA
ENST00000640779.1:c.1862+48_1862+49insAGA
ENST00000405460.6:c.7133+48_7133+49insAGA	ENSP00000384582.2:n.7133+48_7133+49insAGA
NM_032119.3:c.7133+48_7133+49insAGA	NP_115495.3:n.7133+48_7133+49insAGA
NR_003149.1:n.7146+48_7146+49insAGA
XM_011543675.1:c.7130+48_7130+49insAGA	XP_011541977.1:n.7130+48_7130+49insAGA
XM_011543676.1:c.7052+48_7052+49insAGA	XP_011541978.1:n.7052+48_7052+49insAGA
XM_011543677.1:c.4436+48_4436+49insAGA	XP_011541979.1:n.4436+48_4436+49insAGA
XM_011543678.1:c.7133+48_7133+49insAGA	XP_011541980.1:n.7133+48_7133+49insAGA
XM_011543679.1:c.7133+48_7133+49insAGA	XP_011541981.1:n.7133+48_7133+49insAGA
NM_032119.4:c.7133+48_7133+49insAGA MANE Select	NP_115495.3:n.7133+48_7133+49insAGA
XM_017009963.2:c.7133+48_7133+49insAGA	XP_016865452.1:n.7133+48_7133+49insAGA
XM_017009964.2:c.7130+48_7130+49insAGA	XP_016865453.1:n.7130+48_7130+49insAGA
XM_017009965.1:c.7130+48_7130+49insAGA	XP_016865454.1:n.7130+48_7130+49insAGA
XM_017009966.2:c.7052+48_7052+49insAGA	XP_016865455.1:n.7052+48_7052+49insAGA
XM_017009967.1:c.7037+48_7037+49insAGA	XP_016865456.1:n.7037+48_7037+49insAGA
XM_017009968.2:c.7133+48_7133+49insAGA	XP_016865457.1:n.7133+48_7133+49insAGA
XM_017009969.2:c.7133+48_7133+49insAGA	XP_016865458.1:n.7133+48_7133+49insAGA
XM_017009970.2:c.7133+48_7133+49insAGA	XP_016865459.1:n.7133+48_7133+49insAGA
XM_017009971.2:c.7133+48_7133+49insAGA	XP_016865460.1:n.7133+48_7133+49insAGA
XM_017009972.1:c.251+48_251+49insAGA	XP_016865461.1:n.251+48_251+49insAGA
XM_017009973.1:c.251+48_251+49insAGA	XP_016865462.1:n.251+48_251+49insAGA
XM_017009974.2:c.7133+48_7133+49insAGA	XP_016865463.1:n.7133+48_7133+49insAGA
NR_003149.2:n.7149+48_7149+49insAGA