Canonical Allele Identifier: CA1562882067

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745617G= , CM000667.2:g.90745617G=	GRCh38
NC_000005.9:g.90041434G= , CM000667.1:g.90041434G=	GRCh37
NC_000005.8:g.90077190G=	NCBI36
NG_007083.1:g.191818G=
NG_007083.2:g.221274G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10796G= MANE Select	ENSP00000384582.2:p.Gly3599=
ENST00000639431.1:c.265+69408G=	ENSP00000491057.1:n.265+69408G=
ENST00000640374.1:n.3940G=
ENST00000640464.1:n.1215G=
ENST00000405460.6:c.10796G=	ENSP00000384582.2:p.Gly3599=
ENST00000509621.1:c.3493G=
NM_032119.3:c.10796G=	NP_115495.3:p.Gly3599=
NR_003149.1:n.10809G=
XM_011543675.1:c.10793G=	XP_011541977.1:p.Gly3598=
XM_011543676.1:c.10715G=	XP_011541978.1:p.Gly3572=
XM_011543677.1:c.8099G=	XP_011541979.1:p.Gly2700=
XM_011543678.1:c.10796G=	XP_011541980.1:p.Gly3599=
XM_011543679.1:c.*18G=	XP_011541981.1:n.*18G=
NM_032119.4:c.10796G= MANE Select	NP_115495.3:p.Gly3599=
XM_017009963.2:c.10817G=	XP_016865452.1:p.Gly3606=
XM_017009964.2:c.10814G=	XP_016865453.1:p.Gly3605=
XM_017009965.1:c.10814G=	XP_016865454.1:p.Gly3605=
XM_017009966.2:c.10736G=	XP_016865455.1:p.Gly3579=
XM_017009967.1:c.10721G=	XP_016865456.1:p.Gly3574=
XM_017009968.2:c.10817G=	XP_016865457.1:p.Gly3606=
XM_017009969.2:c.10817G=	XP_016865458.1:p.Gly3606=
XM_017009970.2:c.10817G=	XP_016865459.1:p.Gly3606=
XM_017009971.2:c.10817G=	XP_016865460.1:p.Gly3606=
XM_017009972.1:c.3935G=	XP_016865461.1:p.Gly1312=
XM_017009973.1:c.3914G=	XP_016865462.1:p.Gly1305=
XM_017009974.2:c.*18G=	XP_016865463.1:n.*18G=
NR_003149.2:n.10812G=