Canonical Allele Identifier: CA1562873555

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725561A= , CM000667.2:g.90725561A=	GRCh38
NC_000005.9:g.90021378A= , CM000667.1:g.90021378A=	GRCh37
NC_000005.8:g.90057134A=	NCBI36
NG_007083.1:g.171762A=
NG_007083.2:g.201218A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10066A= MANE Select	ENSP00000384582.2:p.Ile3356=
ENST00000639431.1:c.265+49352A=	ENSP00000491057.1:n.265+49352A=
ENST00000640374.1:n.3210A=
ENST00000640464.1:n.485A=
ENST00000405460.6:c.10066A=	ENSP00000384582.2:p.Ile3356=
ENST00000509621.1:c.2763A=
NM_032119.3:c.10066A=	NP_115495.3:p.Ile3356=
NR_003149.1:n.10079A=
XM_011543675.1:c.10063A=	XP_011541977.1:p.Ile3355=
XM_011543676.1:c.9985A=	XP_011541978.1:p.Ile3329=
XM_011543677.1:c.7369A=	XP_011541979.1:p.Ile2457=
XM_011543678.1:c.10066A=	XP_011541980.1:p.Ile3356=
XM_011543679.1:c.10066A=	XP_011541981.1:p.Ile3356=
XR_948560.1:n.272-9752T=
NM_032119.4:c.10066A= MANE Select	NP_115495.3:p.Ile3356=
XM_017009963.2:c.10087A=	XP_016865452.1:p.Ile3363=
XM_017009964.2:c.10084A=	XP_016865453.1:p.Ile3362=
XM_017009965.1:c.10084A=	XP_016865454.1:p.Ile3362=
XM_017009966.2:c.10006A=	XP_016865455.1:p.Ile3336=
XM_017009967.1:c.9991A=	XP_016865456.1:p.Ile3331=
XM_017009968.2:c.10087A=	XP_016865457.1:p.Ile3363=
XM_017009969.2:c.10087A=	XP_016865458.1:p.Ile3363=
XM_017009970.2:c.10087A=	XP_016865459.1:p.Ile3363=
XM_017009971.2:c.10087A=	XP_016865460.1:p.Ile3363=
XM_017009972.1:c.3205A=	XP_016865461.1:p.Ile1069=
XM_017009973.1:c.3184A=	XP_016865462.1:p.Ile1062=
XM_017009974.2:c.10087A=	XP_016865463.1:p.Ile3363=
XR_001742802.1:n.2523-9752T=
NR_003149.2:n.10082A=