Canonical Allele Identifier: CA1078660775

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1746678974
• gnomAD v3: 5-90692966-T-A
• gnomAD v4: 5-90692966-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692966T>A , CM000667.2:g.90692966T>A	GRCh38
NC_000005.9:g.89988783T>A , CM000667.1:g.89988783T>A	GRCh37
NC_000005.8:g.90024539T>A	NCBI36
NG_007083.1:g.139167T>A
NG_007083.2:g.168623T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7133+180T>A MANE Select	ENSP00000384582.2:n.7133+180T>A
ENST00000639431.1:c.265+16757T>A	ENSP00000491057.1:n.265+16757T>A
ENST00000639473.1:n.2592+180T>A
ENST00000640012.1:c.940+180T>A
ENST00000640374.1:n.277+180T>A
ENST00000640403.1:c.4424+180T>A	ENSP00000492531.1:n.4424+180T>A
ENST00000640779.1:c.1862+180T>A
ENST00000405460.6:c.7133+180T>A	ENSP00000384582.2:n.7133+180T>A
NM_032119.3:c.7133+180T>A	NP_115495.3:n.7133+180T>A
NR_003149.1:n.7146+180T>A
XM_011543675.1:c.7130+180T>A	XP_011541977.1:n.7130+180T>A
XM_011543676.1:c.7052+180T>A	XP_011541978.1:n.7052+180T>A
XM_011543677.1:c.4436+180T>A	XP_011541979.1:n.4436+180T>A
XM_011543678.1:c.7133+180T>A	XP_011541980.1:n.7133+180T>A
XM_011543679.1:c.7133+180T>A	XP_011541981.1:n.7133+180T>A
NM_032119.4:c.7133+180T>A MANE Select	NP_115495.3:n.7133+180T>A
XM_017009963.2:c.7133+180T>A	XP_016865452.1:n.7133+180T>A
XM_017009964.2:c.7130+180T>A	XP_016865453.1:n.7130+180T>A
XM_017009965.1:c.7130+180T>A	XP_016865454.1:n.7130+180T>A
XM_017009966.2:c.7052+180T>A	XP_016865455.1:n.7052+180T>A
XM_017009967.1:c.7037+180T>A	XP_016865456.1:n.7037+180T>A
XM_017009968.2:c.7133+180T>A	XP_016865457.1:n.7133+180T>A
XM_017009969.2:c.7133+180T>A	XP_016865458.1:n.7133+180T>A
XM_017009970.2:c.7133+180T>A	XP_016865459.1:n.7133+180T>A
XM_017009971.2:c.7133+180T>A	XP_016865460.1:n.7133+180T>A
XM_017009972.1:c.251+180T>A	XP_016865461.1:n.251+180T>A
XM_017009973.1:c.251+180T>A	XP_016865462.1:n.251+180T>A
XM_017009974.2:c.7133+180T>A	XP_016865463.1:n.7133+180T>A
NR_003149.2:n.7149+180T>A