Canonical Allele Identifier: CA1562859299

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692719C= , CM000667.2:g.90692719C=	GRCh38
NC_000005.9:g.89988536C= , CM000667.1:g.89988536C=	GRCh37
NC_000005.8:g.90024292C=	NCBI36
NG_007083.1:g.138920C=
NG_007083.2:g.168376C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7066C= MANE Select	ENSP00000384582.2:p.Gln2356=
ENST00000639431.1:c.265+16510C=	ENSP00000491057.1:n.265+16510C=
ENST00000639473.1:n.2525C=
ENST00000640012.1:c.873C=
ENST00000640374.1:n.210C=
ENST00000640403.1:c.4357C=	ENSP00000492531.1:p.Gln1453=
ENST00000640779.1:c.1795C=
ENST00000405460.6:c.7066C=	ENSP00000384582.2:p.Gln2356=
NM_032119.3:c.7066C=	NP_115495.3:p.Gln2356=
NR_003149.1:n.7079C=
XM_011543675.1:c.7063C=	XP_011541977.1:p.Gln2355=
XM_011543676.1:c.6985C=	XP_011541978.1:p.Gln2329=
XM_011543677.1:c.4369C=	XP_011541979.1:p.Gln1457=
XM_011543678.1:c.7066C=	XP_011541980.1:p.Gln2356=
XM_011543679.1:c.7066C=	XP_011541981.1:p.Gln2356=
NM_032119.4:c.7066C= MANE Select	NP_115495.3:p.Gln2356=
XM_017009963.2:c.7066C=	XP_016865452.1:p.Gln2356=
XM_017009964.2:c.7063C=	XP_016865453.1:p.Gln2355=
XM_017009965.1:c.7063C=	XP_016865454.1:p.Gln2355=
XM_017009966.2:c.6985C=	XP_016865455.1:p.Gln2329=
XM_017009967.1:c.6970C=	XP_016865456.1:p.Gln2324=
XM_017009968.2:c.7066C=	XP_016865457.1:p.Gln2356=
XM_017009969.2:c.7066C=	XP_016865458.1:p.Gln2356=
XM_017009970.2:c.7066C=	XP_016865459.1:p.Gln2356=
XM_017009971.2:c.7066C=	XP_016865460.1:p.Gln2356=
XM_017009972.1:c.184C=	XP_016865461.1:p.Gln62=
XM_017009973.1:c.184C=	XP_016865462.1:p.Gln62=
XM_017009974.2:c.7066C=	XP_016865463.1:p.Gln2356=
NR_003149.2:n.7082C=