Canonical Allele Identifier: CA445404078

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050882C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755065C>G , CM000667.2:g.90755065C>G	GRCh38
NC_000005.9:g.90050882C>G , CM000667.1:g.90050882C>G	GRCh37
NC_000005.8:g.90086638C>G	NCBI36
NG_007083.1:g.201266C>G
NG_007083.2:g.230722C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11460C>G MANE Select	ENSP00000384582.2:p.Pro3820=
ENST00000425867.3:c.591C>G	ENSP00000392618.3:p.Pro197=
ENST00000639431.1:c.265+78856C>G	ENSP00000491057.1:n.265+78856C>G
ENST00000640374.1:n.4604C>G
ENST00000640464.1:n.1879C>G
ENST00000405460.6:c.11460C>G	ENSP00000384582.2:p.Pro3820=
ENST00000509621.1:c.4157C>G
NM_032119.3:c.11460C>G	NP_115495.3:p.Pro3820=
NR_003149.1:n.11473C>G
XM_011543675.1:c.11457C>G	XP_011541977.1:p.Pro3819=
XM_011543676.1:c.11379C>G	XP_011541978.1:p.Pro3793=
XM_011543677.1:c.8763C>G	XP_011541979.1:p.Pro2921=
XM_011543678.1:c.11460C>G	XP_011541980.1:p.Pro3820=
NM_032119.4:c.11460C>G MANE Select	NP_115495.3:p.Pro3820=
XM_017009963.2:c.11481C>G	XP_016865452.1:p.Pro3827=
XM_017009964.2:c.11478C>G	XP_016865453.1:p.Pro3826=
XM_017009965.1:c.11478C>G	XP_016865454.1:p.Pro3826=
XM_017009966.2:c.11400C>G	XP_016865455.1:p.Pro3800=
XM_017009967.1:c.11385C>G	XP_016865456.1:p.Pro3795=
XM_017009968.2:c.11481C>G	XP_016865457.1:p.Pro3827=
XM_017009969.2:c.11481C>G	XP_016865458.1:p.Pro3827=
XM_017009970.2:c.11481C>G	XP_016865459.1:p.Pro3827=
XM_017009971.2:c.11481C>G	XP_016865460.1:p.Pro3827=
XM_017009972.1:c.4599C>G	XP_016865461.1:p.Pro1533=
XM_017009973.1:c.4578C>G	XP_016865462.1:p.Pro1526=
NR_003149.2:n.11476C>G