Canonical Allele Identifier: CA1562873557

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725566T= , CM000667.2:g.90725566T=	GRCh38
NC_000005.9:g.90021383T= , CM000667.1:g.90021383T=	GRCh37
NC_000005.8:g.90057139T=	NCBI36
NG_007083.1:g.171767T=
NG_007083.2:g.201223T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10071T= MANE Select	ENSP00000384582.2:p.Ile3357=
ENST00000639431.1:c.265+49357T=	ENSP00000491057.1:n.265+49357T=
ENST00000640374.1:n.3215T=
ENST00000640464.1:n.490T=
ENST00000405460.6:c.10071T=	ENSP00000384582.2:p.Ile3357=
ENST00000509621.1:c.2768T=
NM_032119.3:c.10071T=	NP_115495.3:p.Ile3357=
NR_003149.1:n.10084T=
XM_011543675.1:c.10068T=	XP_011541977.1:p.Ile3356=
XM_011543676.1:c.9990T=	XP_011541978.1:p.Ile3330=
XM_011543677.1:c.7374T=	XP_011541979.1:p.Ile2458=
XM_011543678.1:c.10071T=	XP_011541980.1:p.Ile3357=
XM_011543679.1:c.10071T=	XP_011541981.1:p.Ile3357=
XR_948560.1:n.272-9757A=
NM_032119.4:c.10071T= MANE Select	NP_115495.3:p.Ile3357=
XM_017009963.2:c.10092T=	XP_016865452.1:p.Ile3364=
XM_017009964.2:c.10089T=	XP_016865453.1:p.Ile3363=
XM_017009965.1:c.10089T=	XP_016865454.1:p.Ile3363=
XM_017009966.2:c.10011T=	XP_016865455.1:p.Ile3337=
XM_017009967.1:c.9996T=	XP_016865456.1:p.Ile3332=
XM_017009968.2:c.10092T=	XP_016865457.1:p.Ile3364=
XM_017009969.2:c.10092T=	XP_016865458.1:p.Ile3364=
XM_017009970.2:c.10092T=	XP_016865459.1:p.Ile3364=
XM_017009971.2:c.10092T=	XP_016865460.1:p.Ile3364=
XM_017009972.1:c.3210T=	XP_016865461.1:p.Ile1070=
XM_017009973.1:c.3189T=	XP_016865462.1:p.Ile1063=
XM_017009974.2:c.10092T=	XP_016865463.1:p.Ile3364=
XR_001742802.1:n.2523-9757A=
NR_003149.2:n.10087T=