Canonical Allele Identifier: CA1562902281

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791200G= , CM000667.2:g.90791200G=	GRCh38
NC_000005.9:g.90087017G= , CM000667.1:g.90087017G=	GRCh37
NC_000005.8:g.90122773G=	NCBI36
NG_007083.1:g.237401G=
NG_007083.2:g.266857G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14371G= MANE Select	ENSP00000384582.2:p.Ala4791=
ENST00000425867.3:c.3325G=	ENSP00000392618.3:p.Ala1109=
ENST00000507314.2:c.46G=	ENSP00000491299.1:p.Ala16=
ENST00000638510.1:n.1638G=
ENST00000638585.1:n.137G=
ENST00000638975.1:c.1000G=	ENSP00000492630.1:p.Ala334=
ENST00000639431.1:c.265+114991G=	ENSP00000491057.1:n.265+114991G=
ENST00000640407.1:c.781G=	ENSP00000491425.1:p.Ala261=
ENST00000405460.6:c.14371G=	ENSP00000384582.2:p.Ala4791=
ENST00000425867.2:c.1354G=	ENSP00000392618.2:p.Ala452=
ENST00000507314.1:n.46G=
NM_032119.3:c.14371G=	NP_115495.3:p.Ala4791=
NR_003149.1:n.14384G=
XM_011543675.1:c.14368G=	XP_011541977.1:p.Ala4790=
XM_011543676.1:c.14290G=	XP_011541978.1:p.Ala4764=
XM_011543677.1:c.11674G=	XP_011541979.1:p.Ala3892=
XM_011543678.1:c.14371G=	XP_011541980.1:p.Ala4791=
NM_032119.4:c.14371G= MANE Select	NP_115495.3:p.Ala4791=
XM_017009963.2:c.14392G=	XP_016865452.1:p.Ala4798=
XM_017009964.2:c.14389G=	XP_016865453.1:p.Ala4797=
XM_017009965.1:c.14389G=	XP_016865454.1:p.Ala4797=
XM_017009966.2:c.14311G=	XP_016865455.1:p.Ala4771=
XM_017009967.1:c.14296G=	XP_016865456.1:p.Ala4766=
XM_017009968.2:c.14392G=	XP_016865457.1:p.Ala4798=
XM_017009969.2:c.14392G=	XP_016865458.1:p.Ala4798=
XM_017009970.2:c.14392G=	XP_016865459.1:p.Ala4798=
XM_017009971.2:c.14392G=	XP_016865460.1:p.Ala4798=
XM_017009972.1:c.7510G=	XP_016865461.1:p.Ala2504=
XM_017009973.1:c.7489G=	XP_016865462.1:p.Ala2497=
NR_003149.2:n.14387G=