Canonical Allele Identifier: CA2674568741

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90703579-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703579C>A , CM000667.2:g.90703579C>A	GRCh38
NC_000005.9:g.89999396C>A , CM000667.1:g.89999396C>A	GRCh37
NC_000005.8:g.90035152C>A	NCBI36
NG_007083.1:g.149780C>A
NG_007083.2:g.179236C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.8156-86C>A MANE Select	ENSP00000384582.2:n.8156-86C>A
ENST00000639431.1:c.265+27370C>A	ENSP00000491057.1:n.265+27370C>A
ENST00000639473.1:n.3615-86C>A
ENST00000640012.1:c.1963-86C>A
ENST00000640374.1:n.1300-86C>A
ENST00000640403.1:c.5447-86C>A	ENSP00000492531.1:n.5447-86C>A
ENST00000640779.1:c.2885-86C>A
ENST00000405460.6:c.8156-86C>A	ENSP00000384582.2:n.8156-86C>A
ENST00000509621.1:c.853-86C>A
NM_032119.3:c.8156-86C>A	NP_115495.3:n.8156-86C>A
NR_003149.1:n.8169-86C>A
XM_011543675.1:c.8153-86C>A	XP_011541977.1:n.8153-86C>A
XM_011543676.1:c.8075-86C>A	XP_011541978.1:n.8075-86C>A
XM_011543677.1:c.5459-86C>A	XP_011541979.1:n.5459-86C>A
XM_011543678.1:c.8156-86C>A	XP_011541980.1:n.8156-86C>A
XM_011543679.1:c.8156-86C>A	XP_011541981.1:n.8156-86C>A
NM_032119.4:c.8156-86C>A MANE Select	NP_115495.3:n.8156-86C>A
XM_017009963.2:c.8156-86C>A	XP_016865452.1:n.8156-86C>A
XM_017009964.2:c.8153-86C>A	XP_016865453.1:n.8153-86C>A
XM_017009965.1:c.8153-86C>A	XP_016865454.1:n.8153-86C>A
XM_017009966.2:c.8075-86C>A	XP_016865455.1:n.8075-86C>A
XM_017009967.1:c.8060-86C>A	XP_016865456.1:n.8060-86C>A
XM_017009968.2:c.8156-86C>A	XP_016865457.1:n.8156-86C>A
XM_017009969.2:c.8156-86C>A	XP_016865458.1:n.8156-86C>A
XM_017009970.2:c.8156-86C>A	XP_016865459.1:n.8156-86C>A
XM_017009971.2:c.8156-86C>A	XP_016865460.1:n.8156-86C>A
XM_017009972.1:c.1274-86C>A	XP_016865461.1:n.1274-86C>A
XM_017009973.1:c.1274-86C>A	XP_016865462.1:n.1274-86C>A
XM_017009974.2:c.8156-86C>A	XP_016865463.1:n.8156-86C>A
NR_003149.2:n.8172-86C>A