Canonical Allele Identifier: CA2674568679

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90745002-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745002C>A , CM000667.2:g.90745002C>A	GRCh38
NC_000005.9:g.90040819C>A , CM000667.1:g.90040819C>A	GRCh37
NC_000005.8:g.90076575C>A	NCBI36
NG_007083.1:g.191203C>A
NG_007083.2:g.220659C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10550-44C>A MANE Select	ENSP00000384582.2:n.10550-44C>A
ENST00000639431.1:c.265+68793C>A	ENSP00000491057.1:n.265+68793C>A
ENST00000640374.1:n.3694-44C>A
ENST00000640464.1:n.969-44C>A
ENST00000405460.6:c.10550-44C>A	ENSP00000384582.2:n.10550-44C>A
ENST00000509621.1:c.3247-44C>A
NM_032119.3:c.10550-44C>A	NP_115495.3:n.10550-44C>A
NR_003149.1:n.10563-44C>A
XM_011543675.1:c.10547-44C>A	XP_011541977.1:n.10547-44C>A
XM_011543676.1:c.10469-44C>A	XP_011541978.1:n.10469-44C>A
XM_011543677.1:c.7853-44C>A	XP_011541979.1:n.7853-44C>A
XM_011543678.1:c.10550-44C>A	XP_011541980.1:n.10550-44C>A
XM_011543679.1:c.10550-44C>A	XP_011541981.1:n.10550-44C>A
NM_032119.4:c.10550-44C>A MANE Select	NP_115495.3:n.10550-44C>A
XM_017009963.2:c.10571-44C>A	XP_016865452.1:n.10571-44C>A
XM_017009964.2:c.10568-44C>A	XP_016865453.1:n.10568-44C>A
XM_017009965.1:c.10568-44C>A	XP_016865454.1:n.10568-44C>A
XM_017009966.2:c.10490-44C>A	XP_016865455.1:n.10490-44C>A
XM_017009967.1:c.10475-44C>A	XP_016865456.1:n.10475-44C>A
XM_017009968.2:c.10571-44C>A	XP_016865457.1:n.10571-44C>A
XM_017009969.2:c.10571-44C>A	XP_016865458.1:n.10571-44C>A
XM_017009970.2:c.10571-44C>A	XP_016865459.1:n.10571-44C>A
XM_017009971.2:c.10571-44C>A	XP_016865460.1:n.10571-44C>A
XM_017009972.1:c.3689-44C>A	XP_016865461.1:n.3689-44C>A
XM_017009973.1:c.3668-44C>A	XP_016865462.1:n.3668-44C>A
XM_017009974.2:c.10571-44C>A	XP_016865463.1:n.10571-44C>A
NR_003149.2:n.10566-44C>A