Canonical Allele Identifier: CA3341757

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90802774A>G , CM000667.2:g.90802774A>G	GRCh38
NC_000005.9:g.90098591A>G , CM000667.1:g.90098591A>G	GRCh37
NC_000005.8:g.90134347A>G	NCBI36
NG_007083.1:g.248975A>G
NG_007083.2:g.278431A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14553A>G MANE Select	NP_115495.3:p.Gln4851=
ENST00000405460.9:c.14553A>G MANE Select	ENSP00000384582.2:p.Gln4851=
NM_032119.3:c.14553A>G	NP_115495.3:p.Gln4851=
NR_003149.1:n.14566A>G
NR_003149.2:n.14569A>G
ENST00000405460.6:c.14553A>G	ENSP00000384582.2:p.Gln4851=
ENST00000425867.2:c.1536A>G	ENSP00000392618.2:p.Gln512=
ENST00000425867.3:c.3507A>G	ENSP00000392618.3:p.Gln1169=
ENST00000638510.1:n.1820A>G
ENST00000638585.1:n.319A>G
ENST00000639431.1:c.265+126565A>G	ENSP00000491057.1:n.265+126565A>G
ENST00000640407.1:c.963A>G	ENSP00000491425.1:p.Gln321=
XM_011543675.1:c.14550A>G	XP_011541977.1:p.Gln4850=
XM_011543676.1:c.14472A>G	XP_011541978.1:p.Gln4824=
XM_011543677.1:c.11856A>G	XP_011541979.1:p.Gln3952=
XM_011543678.1:c.14553A>G	XP_011541980.1:p.Gln4851=
XM_017009963.2:c.14574A>G	XP_016865452.1:p.Gln4858=
XM_017009964.2:c.14571A>G	XP_016865453.1:p.Gln4857=
XM_017009965.1:c.14571A>G	XP_016865454.1:p.Gln4857=
XM_017009966.2:c.14493A>G	XP_016865455.1:p.Gln4831=
XM_017009967.1:c.14478A>G	XP_016865456.1:p.Gln4826=
XM_017009968.2:c.14574A>G	XP_016865457.1:p.Gln4858=
XM_017009969.2:c.14574A>G	XP_016865458.1:p.Gln4858=
XM_017009970.2:c.14574A>G	XP_016865459.1:p.Gln4858=
XM_017009971.2:c.14574A>G	XP_016865460.1:p.Gln4858=
XM_017009972.1:c.7692A>G	XP_016865461.1:p.Gln2564=
XM_017009973.1:c.7671A>G	XP_016865462.1:p.Gln2557=