Canonical Allele Identifier: CA1562882081

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745637G= , CM000667.2:g.90745637G=	GRCh38
NC_000005.9:g.90041454G= , CM000667.1:g.90041454G=	GRCh37
NC_000005.8:g.90077210G=	NCBI36
NG_007083.1:g.191838G=
NG_007083.2:g.221294G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10816G= MANE Select	ENSP00000384582.2:p.Ala3606=
ENST00000639431.1:c.265+69428G=	ENSP00000491057.1:n.265+69428G=
ENST00000640374.1:n.3960G=
ENST00000640464.1:n.1235G=
ENST00000405460.6:c.10816G=	ENSP00000384582.2:p.Ala3606=
ENST00000509621.1:c.3513G=
NM_032119.3:c.10816G=	NP_115495.3:p.Ala3606=
NR_003149.1:n.10829G=
XM_011543675.1:c.10813G=	XP_011541977.1:p.Ala3605=
XM_011543676.1:c.10735G=	XP_011541978.1:p.Ala3579=
XM_011543677.1:c.8119G=	XP_011541979.1:p.Ala2707=
XM_011543678.1:c.10816G=	XP_011541980.1:p.Ala3606=
XM_011543679.1:c.*38G=	XP_011541981.1:n.*38G=
NM_032119.4:c.10816G= MANE Select	NP_115495.3:p.Ala3606=
XM_017009963.2:c.10837G=	XP_016865452.1:p.Ala3613=
XM_017009964.2:c.10834G=	XP_016865453.1:p.Ala3612=
XM_017009965.1:c.10834G=	XP_016865454.1:p.Ala3612=
XM_017009966.2:c.10756G=	XP_016865455.1:p.Ala3586=
XM_017009967.1:c.10741G=	XP_016865456.1:p.Ala3581=
XM_017009968.2:c.10837G=	XP_016865457.1:p.Ala3613=
XM_017009969.2:c.10837G=	XP_016865458.1:p.Ala3613=
XM_017009970.2:c.10837G=	XP_016865459.1:p.Ala3613=
XM_017009971.2:c.10837G=	XP_016865460.1:p.Ala3613=
XM_017009972.1:c.3955G=	XP_016865461.1:p.Ala1319=
XM_017009973.1:c.3934G=	XP_016865462.1:p.Ala1312=
XM_017009974.2:c.*38G=	XP_016865463.1:n.*38G=
NR_003149.2:n.10832G=