Canonical Allele Identifier: CA1562882077

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745632C= , CM000667.2:g.90745632C=	GRCh38
NC_000005.9:g.90041449C= , CM000667.1:g.90041449C=	GRCh37
NC_000005.8:g.90077205C=	NCBI36
NG_007083.1:g.191833C=
NG_007083.2:g.221289C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10811C= MANE Select	ENSP00000384582.2:p.Thr3604=
ENST00000639431.1:c.265+69423C=	ENSP00000491057.1:n.265+69423C=
ENST00000640374.1:n.3955C=
ENST00000640464.1:n.1230C=
ENST00000405460.6:c.10811C=	ENSP00000384582.2:p.Thr3604=
ENST00000509621.1:c.3508C=
NM_032119.3:c.10811C=	NP_115495.3:p.Thr3604=
NR_003149.1:n.10824C=
XM_011543675.1:c.10808C=	XP_011541977.1:p.Thr3603=
XM_011543676.1:c.10730C=	XP_011541978.1:p.Thr3577=
XM_011543677.1:c.8114C=	XP_011541979.1:p.Thr2705=
XM_011543678.1:c.10811C=	XP_011541980.1:p.Thr3604=
XM_011543679.1:c.*33C=	XP_011541981.1:n.*33C=
NM_032119.4:c.10811C= MANE Select	NP_115495.3:p.Thr3604=
XM_017009963.2:c.10832C=	XP_016865452.1:p.Thr3611=
XM_017009964.2:c.10829C=	XP_016865453.1:p.Thr3610=
XM_017009965.1:c.10829C=	XP_016865454.1:p.Thr3610=
XM_017009966.2:c.10751C=	XP_016865455.1:p.Thr3584=
XM_017009967.1:c.10736C=	XP_016865456.1:p.Thr3579=
XM_017009968.2:c.10832C=	XP_016865457.1:p.Thr3611=
XM_017009969.2:c.10832C=	XP_016865458.1:p.Thr3611=
XM_017009970.2:c.10832C=	XP_016865459.1:p.Thr3611=
XM_017009971.2:c.10832C=	XP_016865460.1:p.Thr3611=
XM_017009972.1:c.3950C=	XP_016865461.1:p.Thr1317=
XM_017009973.1:c.3929C=	XP_016865462.1:p.Thr1310=
XM_017009974.2:c.*33C=	XP_016865463.1:n.*33C=
NR_003149.2:n.10827C=