Canonical Allele Identifier: CA445404507

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988496T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692679T>A , CM000667.2:g.90692679T>A	GRCh38
NC_000005.9:g.89988496T>A , CM000667.1:g.89988496T>A	GRCh37
NC_000005.8:g.90024252T>A	NCBI36
NG_007083.1:g.138880T>A
NG_007083.2:g.168336T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7026T>A MANE Select	ENSP00000384582.2:p.Ile2342=
ENST00000639431.1:c.265+16470T>A	ENSP00000491057.1:n.265+16470T>A
ENST00000639473.1:n.2485T>A
ENST00000640012.1:c.833T>A
ENST00000640374.1:n.170T>A
ENST00000640403.1:c.4317T>A	ENSP00000492531.1:p.Ile1439=
ENST00000640779.1:c.1755T>A
ENST00000405460.6:c.7026T>A	ENSP00000384582.2:p.Ile2342=
NM_032119.3:c.7026T>A	NP_115495.3:p.Ile2342=
NR_003149.1:n.7039T>A
XM_011543675.1:c.7023T>A	XP_011541977.1:p.Ile2341=
XM_011543676.1:c.6945T>A	XP_011541978.1:p.Ile2315=
XM_011543677.1:c.4329T>A	XP_011541979.1:p.Ile1443=
XM_011543678.1:c.7026T>A	XP_011541980.1:p.Ile2342=
XM_011543679.1:c.7026T>A	XP_011541981.1:p.Ile2342=
NM_032119.4:c.7026T>A MANE Select	NP_115495.3:p.Ile2342=
XM_017009963.2:c.7026T>A	XP_016865452.1:p.Ile2342=
XM_017009964.2:c.7023T>A	XP_016865453.1:p.Ile2341=
XM_017009965.1:c.7023T>A	XP_016865454.1:p.Ile2341=
XM_017009966.2:c.6945T>A	XP_016865455.1:p.Ile2315=
XM_017009967.1:c.6930T>A	XP_016865456.1:p.Ile2310=
XM_017009968.2:c.7026T>A	XP_016865457.1:p.Ile2342=
XM_017009969.2:c.7026T>A	XP_016865458.1:p.Ile2342=
XM_017009970.2:c.7026T>A	XP_016865459.1:p.Ile2342=
XM_017009971.2:c.7026T>A	XP_016865460.1:p.Ile2342=
XM_017009972.1:c.144T>A	XP_016865461.1:p.Ile48=
XM_017009973.1:c.144T>A	XP_016865462.1:p.Ile48=
XM_017009974.2:c.7026T>A	XP_016865463.1:p.Ile2342=
NR_003149.2:n.7042T>A