Canonical Allele Identifier: CA3340627

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725085G>A , CM000667.2:g.90725085G>A	GRCh38
NC_000005.9:g.90020902G>A , CM000667.1:g.90020902G>A	GRCh37
NC_000005.8:g.90056658G>A	NCBI36
NG_007083.1:g.171286G>A
NG_007083.2:g.200742G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9907-1G>A MANE Select	NP_115495.3:n.9907-1G>A
ENST00000405460.9:c.9907-1G>A MANE Select	ENSP00000384582.2:n.9907-1G>A
NM_032119.3:c.9907-1G>A	NP_115495.3:n.9907-1G>A
NR_003149.1:n.9920-1G>A
NR_003149.2:n.9923-1G>A
ENST00000405460.6:c.9907-1G>A	ENSP00000384582.2:n.9907-1G>A
ENST00000509621.1:c.2604-1G>A
ENST00000639431.1:c.265+48876G>A	ENSP00000491057.1:n.265+48876G>A
ENST00000640374.1:n.3051-1G>A
ENST00000640464.1:n.326-1G>A
ENST00000640779.1:c.4636-1G>A
XM_011543675.1:c.9904-1G>A	XP_011541977.1:n.9904-1G>A
XM_011543676.1:c.9826-1G>A	XP_011541978.1:n.9826-1G>A
XM_011543677.1:c.7210-1G>A	XP_011541979.1:n.7210-1G>A
XM_011543678.1:c.9907-1G>A	XP_011541980.1:n.9907-1G>A
XM_011543679.1:c.9907-1G>A	XP_011541981.1:n.9907-1G>A
XM_017009963.2:c.9928-1G>A	XP_016865452.1:n.9928-1G>A
XM_017009964.2:c.9925-1G>A	XP_016865453.1:n.9925-1G>A
XM_017009965.1:c.9925-1G>A	XP_016865454.1:n.9925-1G>A
XM_017009966.2:c.9847-1G>A	XP_016865455.1:n.9847-1G>A
XM_017009967.1:c.9832-1G>A	XP_016865456.1:n.9832-1G>A
XM_017009968.2:c.9928-1G>A	XP_016865457.1:n.9928-1G>A
XM_017009969.2:c.9928-1G>A	XP_016865458.1:n.9928-1G>A
XM_017009970.2:c.9928-1G>A	XP_016865459.1:n.9928-1G>A
XM_017009971.2:c.9928-1G>A	XP_016865460.1:n.9928-1G>A
XM_017009972.1:c.3046-1G>A	XP_016865461.1:n.3046-1G>A
XM_017009973.1:c.3025-1G>A	XP_016865462.1:n.3025-1G>A
XM_017009974.2:c.9928-1G>A	XP_016865463.1:n.9928-1G>A
XR_001742802.1:n.2523-9276C>T
XR_948560.1:n.272-9276C>T