Canonical Allele Identifier: CA1562886201

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755092A= , CM000667.2:g.90755092A=	GRCh38
NC_000005.9:g.90050909A= , CM000667.1:g.90050909A=	GRCh37
NC_000005.8:g.90086665A=	NCBI36
NG_007083.1:g.201293A=
NG_007083.2:g.230749A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11487A= MANE Select	ENSP00000384582.2:p.Gln3829=
ENST00000425867.3:c.618A=	ENSP00000392618.3:p.Gln206=
ENST00000639431.1:c.265+78883A=	ENSP00000491057.1:n.265+78883A=
ENST00000640374.1:n.4631A=
ENST00000640464.1:n.1906A=
ENST00000405460.6:c.11487A=	ENSP00000384582.2:p.Gln3829=
ENST00000509621.1:c.4184A=
NM_032119.3:c.11487A=	NP_115495.3:p.Gln3829=
NR_003149.1:n.11500A=
XM_011543675.1:c.11484A=	XP_011541977.1:p.Gln3828=
XM_011543676.1:c.11406A=	XP_011541978.1:p.Gln3802=
XM_011543677.1:c.8790A=	XP_011541979.1:p.Gln2930=
XM_011543678.1:c.11487A=	XP_011541980.1:p.Gln3829=
NM_032119.4:c.11487A= MANE Select	NP_115495.3:p.Gln3829=
XM_017009963.2:c.11508A=	XP_016865452.1:p.Gln3836=
XM_017009964.2:c.11505A=	XP_016865453.1:p.Gln3835=
XM_017009965.1:c.11505A=	XP_016865454.1:p.Gln3835=
XM_017009966.2:c.11427A=	XP_016865455.1:p.Gln3809=
XM_017009967.1:c.11412A=	XP_016865456.1:p.Gln3804=
XM_017009968.2:c.11508A=	XP_016865457.1:p.Gln3836=
XM_017009969.2:c.11508A=	XP_016865458.1:p.Gln3836=
XM_017009970.2:c.11508A=	XP_016865459.1:p.Gln3836=
XM_017009971.2:c.11508A=	XP_016865460.1:p.Gln3836=
XM_017009972.1:c.4626A=	XP_016865461.1:p.Gln1542=
XM_017009973.1:c.4605A=	XP_016865462.1:p.Gln1535=
NR_003149.2:n.11503A=