Canonical Allele Identifier: CA1562882083

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745641T= , CM000667.2:g.90745641T=	GRCh38
NC_000005.9:g.90041458T= , CM000667.1:g.90041458T=	GRCh37
NC_000005.8:g.90077214T=	NCBI36
NG_007083.1:g.191842T=
NG_007083.2:g.221298T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10820T= MANE Select	ENSP00000384582.2:p.Val3607=
ENST00000639431.1:c.265+69432T=	ENSP00000491057.1:n.265+69432T=
ENST00000640374.1:n.3964T=
ENST00000640464.1:n.1239T=
ENST00000405460.6:c.10820T=	ENSP00000384582.2:p.Val3607=
ENST00000509621.1:c.3517T=
NM_032119.3:c.10820T=	NP_115495.3:p.Val3607=
NR_003149.1:n.10833T=
XM_011543675.1:c.10817T=	XP_011541977.1:p.Val3606=
XM_011543676.1:c.10739T=	XP_011541978.1:p.Val3580=
XM_011543677.1:c.8123T=	XP_011541979.1:p.Val2708=
XM_011543678.1:c.10820T=	XP_011541980.1:p.Val3607=
XM_011543679.1:c.*42T=	XP_011541981.1:n.*42T=
NM_032119.4:c.10820T= MANE Select	NP_115495.3:p.Val3607=
XM_017009963.2:c.10841T=	XP_016865452.1:p.Val3614=
XM_017009964.2:c.10838T=	XP_016865453.1:p.Val3613=
XM_017009965.1:c.10838T=	XP_016865454.1:p.Val3613=
XM_017009966.2:c.10760T=	XP_016865455.1:p.Val3587=
XM_017009967.1:c.10745T=	XP_016865456.1:p.Val3582=
XM_017009968.2:c.10841T=	XP_016865457.1:p.Val3614=
XM_017009969.2:c.10841T=	XP_016865458.1:p.Val3614=
XM_017009970.2:c.10841T=	XP_016865459.1:p.Val3614=
XM_017009971.2:c.10841T=	XP_016865460.1:p.Val3614=
XM_017009972.1:c.3959T=	XP_016865461.1:p.Val1320=
XM_017009973.1:c.3938T=	XP_016865462.1:p.Val1313=
XM_017009974.2:c.*42T=	XP_016865463.1:n.*42T=
NR_003149.2:n.10836T=