Canonical Allele Identifier: CA445404020

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050843A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755026A>G , CM000667.2:g.90755026A>G	GRCh38
NC_000005.9:g.90050843A>G , CM000667.1:g.90050843A>G	GRCh37
NC_000005.8:g.90086599A>G	NCBI36
NG_007083.1:g.201227A>G
NG_007083.2:g.230683A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11421A>G MANE Select	ENSP00000384582.2:p.Gly3807=
ENST00000425867.3:c.552A>G	ENSP00000392618.3:p.Gly184=
ENST00000639431.1:c.265+78817A>G	ENSP00000491057.1:n.265+78817A>G
ENST00000640374.1:n.4565A>G
ENST00000640464.1:n.1840A>G
ENST00000405460.6:c.11421A>G	ENSP00000384582.2:p.Gly3807=
ENST00000509621.1:c.4118A>G
NM_032119.3:c.11421A>G	NP_115495.3:p.Gly3807=
NR_003149.1:n.11434A>G
XM_011543675.1:c.11418A>G	XP_011541977.1:p.Gly3806=
XM_011543676.1:c.11340A>G	XP_011541978.1:p.Gly3780=
XM_011543677.1:c.8724A>G	XP_011541979.1:p.Gly2908=
XM_011543678.1:c.11421A>G	XP_011541980.1:p.Gly3807=
NM_032119.4:c.11421A>G MANE Select	NP_115495.3:p.Gly3807=
XM_017009963.2:c.11442A>G	XP_016865452.1:p.Gly3814=
XM_017009964.2:c.11439A>G	XP_016865453.1:p.Gly3813=
XM_017009965.1:c.11439A>G	XP_016865454.1:p.Gly3813=
XM_017009966.2:c.11361A>G	XP_016865455.1:p.Gly3787=
XM_017009967.1:c.11346A>G	XP_016865456.1:p.Gly3782=
XM_017009968.2:c.11442A>G	XP_016865457.1:p.Gly3814=
XM_017009969.2:c.11442A>G	XP_016865458.1:p.Gly3814=
XM_017009970.2:c.11442A>G	XP_016865459.1:p.Gly3814=
XM_017009971.2:c.11442A>G	XP_016865460.1:p.Gly3814=
XM_017009972.1:c.4560A>G	XP_016865461.1:p.Gly1520=
XM_017009973.1:c.4539A>G	XP_016865462.1:p.Gly1513=
NR_003149.2:n.11437A>G