Canonical Allele Identifier: CA3341294

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90777990T>G , CM000667.2:g.90777990T>G	GRCh38
NC_000005.9:g.90073807T>G , CM000667.1:g.90073807T>G	GRCh37
NC_000005.8:g.90109563T>G	NCBI36
NG_007083.1:g.224191T>G
NG_007083.2:g.253647T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12613T>G MANE Select	NP_115495.3:p.Ser4205Ala
ENST00000405460.9:c.12613T>G MANE Select	ENSP00000384582.2:p.Ser4205Ala
NM_032119.3:c.12613T>G	NP_115495.3:p.Ser4205Ala
NR_003149.1:n.12626T>G
NR_003149.2:n.12629T>G
ENST00000405460.6:c.12613T>G	ENSP00000384582.2:p.Ser4205Ala
ENST00000425867.3:c.1567T>G	ENSP00000392618.3:p.Ser523Ala
ENST00000639431.1:c.265+101781T>G	ENSP00000491057.1:n.265+101781T>G
ENST00000640464.1:n.3032T>G
ENST00000640729.1:n.1190T>G
XM_011543675.1:c.12610T>G	XP_011541977.1:p.Ser4204Ala
XM_011543676.1:c.12532T>G	XP_011541978.1:p.Ser4178Ala
XM_011543677.1:c.9916T>G	XP_011541979.1:p.Ser3306Ala
XM_011543678.1:c.12613T>G	XP_011541980.1:p.Ser4205Ala
XM_017009963.2:c.12634T>G	XP_016865452.1:p.Ser4212Ala
XM_017009964.2:c.12631T>G	XP_016865453.1:p.Ser4211Ala
XM_017009965.1:c.12631T>G	XP_016865454.1:p.Ser4211Ala
XM_017009966.2:c.12553T>G	XP_016865455.1:p.Ser4185Ala
XM_017009967.1:c.12538T>G	XP_016865456.1:p.Ser4180Ala
XM_017009968.2:c.12634T>G	XP_016865457.1:p.Ser4212Ala
XM_017009969.2:c.12634T>G	XP_016865458.1:p.Ser4212Ala
XM_017009970.2:c.12634T>G	XP_016865459.1:p.Ser4212Ala
XM_017009971.2:c.12634T>G	XP_016865460.1:p.Ser4212Ala
XM_017009972.1:c.5752T>G	XP_016865461.1:p.Ser1918Ala
XM_017009973.1:c.5731T>G	XP_016865462.1:p.Ser1911Ala