Canonical Allele Identifier: CA1562882056

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745594A= , CM000667.2:g.90745594A=	GRCh38
NC_000005.9:g.90041411A= , CM000667.1:g.90041411A=	GRCh37
NC_000005.8:g.90077167A=	NCBI36
NG_007083.1:g.191795A=
NG_007083.2:g.221251A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10773A= MANE Select	ENSP00000384582.2:p.Ser3591=
ENST00000639431.1:c.265+69385A=	ENSP00000491057.1:n.265+69385A=
ENST00000640374.1:n.3917A=
ENST00000640464.1:n.1192A=
ENST00000405460.6:c.10773A=	ENSP00000384582.2:p.Ser3591=
ENST00000509621.1:c.3470A=
NM_032119.3:c.10773A=	NP_115495.3:p.Ser3591=
NR_003149.1:n.10786A=
XM_011543675.1:c.10770A=	XP_011541977.1:p.Ser3590=
XM_011543676.1:c.10692A=	XP_011541978.1:p.Ser3564=
XM_011543677.1:c.8076A=	XP_011541979.1:p.Ser2692=
XM_011543678.1:c.10773A=	XP_011541980.1:p.Ser3591=
XM_011543679.1:c.10770-2A=	XP_011541981.1:n.10770-2A=
NM_032119.4:c.10773A= MANE Select	NP_115495.3:p.Ser3591=
XM_017009963.2:c.10794A=	XP_016865452.1:p.Ser3598=
XM_017009964.2:c.10791A=	XP_016865453.1:p.Ser3597=
XM_017009965.1:c.10791A=	XP_016865454.1:p.Ser3597=
XM_017009966.2:c.10713A=	XP_016865455.1:p.Ser3571=
XM_017009967.1:c.10698A=	XP_016865456.1:p.Ser3566=
XM_017009968.2:c.10794A=	XP_016865457.1:p.Ser3598=
XM_017009969.2:c.10794A=	XP_016865458.1:p.Ser3598=
XM_017009970.2:c.10794A=	XP_016865459.1:p.Ser3598=
XM_017009971.2:c.10794A=	XP_016865460.1:p.Ser3598=
XM_017009972.1:c.3912A=	XP_016865461.1:p.Ser1304=
XM_017009973.1:c.3891A=	XP_016865462.1:p.Ser1297=
XM_017009974.2:c.10791-2A=	XP_016865463.1:n.10791-2A=
NR_003149.2:n.10789A=