Canonical Allele Identifier: CA1562859950

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90694332A= , CM000667.2:g.90694332A=	GRCh38
NC_000005.9:g.89990149A= , CM000667.1:g.89990149A=	GRCh37
NC_000005.8:g.90025905A=	NCBI36
NG_007083.1:g.140533A=
NG_007083.2:g.169989A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7576A= MANE Select	ENSP00000384582.2:p.Ile2526=
ENST00000639431.1:c.265+18123A=	ENSP00000491057.1:n.265+18123A=
ENST00000639473.1:n.3035A=
ENST00000640012.1:c.1383A=
ENST00000640374.1:n.720A=
ENST00000640403.1:c.4867A=	ENSP00000492531.1:p.Ile1623=
ENST00000640779.1:c.2305A=
ENST00000405460.6:c.7576A=	ENSP00000384582.2:p.Ile2526=
ENST00000509621.1:c.273A=
NM_032119.3:c.7576A=	NP_115495.3:p.Ile2526=
NR_003149.1:n.7589A=
XM_011543675.1:c.7573A=	XP_011541977.1:p.Ile2525=
XM_011543676.1:c.7495A=	XP_011541978.1:p.Ile2499=
XM_011543677.1:c.4879A=	XP_011541979.1:p.Ile1627=
XM_011543678.1:c.7576A=	XP_011541980.1:p.Ile2526=
XM_011543679.1:c.7576A=	XP_011541981.1:p.Ile2526=
NM_032119.4:c.7576A= MANE Select	NP_115495.3:p.Ile2526=
XM_017009963.2:c.7576A=	XP_016865452.1:p.Ile2526=
XM_017009964.2:c.7573A=	XP_016865453.1:p.Ile2525=
XM_017009965.1:c.7573A=	XP_016865454.1:p.Ile2525=
XM_017009966.2:c.7495A=	XP_016865455.1:p.Ile2499=
XM_017009967.1:c.7480A=	XP_016865456.1:p.Ile2494=
XM_017009968.2:c.7576A=	XP_016865457.1:p.Ile2526=
XM_017009969.2:c.7576A=	XP_016865458.1:p.Ile2526=
XM_017009970.2:c.7576A=	XP_016865459.1:p.Ile2526=
XM_017009971.2:c.7576A=	XP_016865460.1:p.Ile2526=
XM_017009972.1:c.694A=	XP_016865461.1:p.Ile232=
XM_017009973.1:c.694A=	XP_016865462.1:p.Ile232=
XM_017009974.2:c.7576A=	XP_016865463.1:p.Ile2526=
NR_003149.2:n.7592A=