Canonical Allele Identifier: CA2674568756

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90703608-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703608C>G , CM000667.2:g.90703608C>G	GRCh38
NC_000005.9:g.89999425C>G , CM000667.1:g.89999425C>G	GRCh37
NC_000005.8:g.90035181C>G	NCBI36
NG_007083.1:g.149809C>G
NG_007083.2:g.179265C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.8156-57C>G MANE Select	ENSP00000384582.2:n.8156-57C>G
ENST00000639431.1:c.265+27399C>G	ENSP00000491057.1:n.265+27399C>G
ENST00000639473.1:n.3615-57C>G
ENST00000640012.1:c.1963-57C>G
ENST00000640374.1:n.1300-57C>G
ENST00000640403.1:c.5447-57C>G	ENSP00000492531.1:n.5447-57C>G
ENST00000640779.1:c.2885-57C>G
ENST00000405460.6:c.8156-57C>G	ENSP00000384582.2:n.8156-57C>G
ENST00000509621.1:c.853-57C>G
NM_032119.3:c.8156-57C>G	NP_115495.3:n.8156-57C>G
NR_003149.1:n.8169-57C>G
XM_011543675.1:c.8153-57C>G	XP_011541977.1:n.8153-57C>G
XM_011543676.1:c.8075-57C>G	XP_011541978.1:n.8075-57C>G
XM_011543677.1:c.5459-57C>G	XP_011541979.1:n.5459-57C>G
XM_011543678.1:c.8156-57C>G	XP_011541980.1:n.8156-57C>G
XM_011543679.1:c.8156-57C>G	XP_011541981.1:n.8156-57C>G
NM_032119.4:c.8156-57C>G MANE Select	NP_115495.3:n.8156-57C>G
XM_017009963.2:c.8156-57C>G	XP_016865452.1:n.8156-57C>G
XM_017009964.2:c.8153-57C>G	XP_016865453.1:n.8153-57C>G
XM_017009965.1:c.8153-57C>G	XP_016865454.1:n.8153-57C>G
XM_017009966.2:c.8075-57C>G	XP_016865455.1:n.8075-57C>G
XM_017009967.1:c.8060-57C>G	XP_016865456.1:n.8060-57C>G
XM_017009968.2:c.8156-57C>G	XP_016865457.1:n.8156-57C>G
XM_017009969.2:c.8156-57C>G	XP_016865458.1:n.8156-57C>G
XM_017009970.2:c.8156-57C>G	XP_016865459.1:n.8156-57C>G
XM_017009971.2:c.8156-57C>G	XP_016865460.1:n.8156-57C>G
XM_017009972.1:c.1274-57C>G	XP_016865461.1:n.1274-57C>G
XM_017009973.1:c.1274-57C>G	XP_016865462.1:n.1274-57C>G
XM_017009974.2:c.8156-57C>G	XP_016865463.1:n.8156-57C>G
NR_003149.2:n.8172-57C>G