Canonical Allele Identifier: CA3341715

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791202T>A , CM000667.2:g.90791202T>A	GRCh38
NC_000005.9:g.90087019T>A , CM000667.1:g.90087019T>A	GRCh37
NC_000005.8:g.90122775T>A	NCBI36
NG_007083.1:g.237403T>A
NG_007083.2:g.266859T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14373T>A MANE Select	NP_115495.3:p.Ala4791=
ENST00000405460.9:c.14373T>A MANE Select	ENSP00000384582.2:p.Ala4791=
NM_032119.3:c.14373T>A	NP_115495.3:p.Ala4791=
NR_003149.1:n.14386T>A
NR_003149.2:n.14389T>A
ENST00000405460.6:c.14373T>A	ENSP00000384582.2:p.Ala4791=
ENST00000425867.2:c.1356T>A	ENSP00000392618.2:p.Ala452=
ENST00000425867.3:c.3327T>A	ENSP00000392618.3:p.Ala1109=
ENST00000507314.1:n.48T>A
ENST00000507314.2:c.48T>A	ENSP00000491299.1:p.Ala16=
ENST00000638510.1:n.1640T>A
ENST00000638585.1:n.139T>A
ENST00000638975.1:c.1002T>A	ENSP00000492630.1:p.Ala334=
ENST00000639431.1:c.265+114993T>A	ENSP00000491057.1:n.265+114993T>A
ENST00000640407.1:c.783T>A	ENSP00000491425.1:p.Ala261=
XM_011543675.1:c.14370T>A	XP_011541977.1:p.Ala4790=
XM_011543676.1:c.14292T>A	XP_011541978.1:p.Ala4764=
XM_011543677.1:c.11676T>A	XP_011541979.1:p.Ala3892=
XM_011543678.1:c.14373T>A	XP_011541980.1:p.Ala4791=
XM_017009963.2:c.14394T>A	XP_016865452.1:p.Ala4798=
XM_017009964.2:c.14391T>A	XP_016865453.1:p.Ala4797=
XM_017009965.1:c.14391T>A	XP_016865454.1:p.Ala4797=
XM_017009966.2:c.14313T>A	XP_016865455.1:p.Ala4771=
XM_017009967.1:c.14298T>A	XP_016865456.1:p.Ala4766=
XM_017009968.2:c.14394T>A	XP_016865457.1:p.Ala4798=
XM_017009969.2:c.14394T>A	XP_016865458.1:p.Ala4798=
XM_017009970.2:c.14394T>A	XP_016865459.1:p.Ala4798=
XM_017009971.2:c.14394T>A	XP_016865460.1:p.Ala4798=
XM_017009972.1:c.7512T>A	XP_016865461.1:p.Ala2504=
XM_017009973.1:c.7491T>A	XP_016865462.1:p.Ala2497=