Canonical Allele Identifier: CA360365566

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90753830G>A , CM000667.2:g.90753830G>A	GRCh38
NC_000005.9:g.90049647G>A , CM000667.1:g.90049647G>A	GRCh37
NC_000005.8:g.90085403G>A	NCBI36
NG_007083.1:g.200031G>A
NG_007083.2:g.229487G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11377+1G>A MANE Select	NP_115495.3:n.11377+1G>A
ENST00000405460.9:c.11377+1G>A MANE Select	ENSP00000384582.2:n.11377+1G>A
NM_032119.3:c.11377+1G>A	NP_115495.3:n.11377+1G>A
NR_003149.1:n.11390+1G>A
NR_003149.2:n.11393+1G>A
ENST00000405460.6:c.11377+1G>A	ENSP00000384582.2:n.11377+1G>A
ENST00000425867.3:c.508+1G>A	ENSP00000392618.3:n.508+1G>A
ENST00000509621.1:c.4074+1G>A
ENST00000639431.1:c.265+77621G>A	ENSP00000491057.1:n.265+77621G>A
ENST00000640374.1:n.4521+1G>A
ENST00000640464.1:n.1796+1G>A
XM_011543675.1:c.11374+1G>A	XP_011541977.1:n.11374+1G>A
XM_011543676.1:c.11296+1G>A	XP_011541978.1:n.11296+1G>A
XM_011543677.1:c.8680+1G>A	XP_011541979.1:n.8680+1G>A
XM_011543678.1:c.11377+1G>A	XP_011541980.1:n.11377+1G>A
XM_017009963.2:c.11398+1G>A	XP_016865452.1:n.11398+1G>A
XM_017009964.2:c.11395+1G>A	XP_016865453.1:n.11395+1G>A
XM_017009965.1:c.11395+1G>A	XP_016865454.1:n.11395+1G>A
XM_017009966.2:c.11317+1G>A	XP_016865455.1:n.11317+1G>A
XM_017009967.1:c.11302+1G>A	XP_016865456.1:n.11302+1G>A
XM_017009968.2:c.11398+1G>A	XP_016865457.1:n.11398+1G>A
XM_017009969.2:c.11398+1G>A	XP_016865458.1:n.11398+1G>A
XM_017009970.2:c.11398+1G>A	XP_016865459.1:n.11398+1G>A
XM_017009971.2:c.11398+1G>A	XP_016865460.1:n.11398+1G>A
XM_017009972.1:c.4516+1G>A	XP_016865461.1:n.4516+1G>A
XM_017009973.1:c.4495+1G>A	XP_016865462.1:n.4495+1G>A