Canonical Allele Identifier: CA1562886230

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755163A= , CM000667.2:g.90755163A=	GRCh38
NC_000005.9:g.90050980A= , CM000667.1:g.90050980A=	GRCh37
NC_000005.8:g.90086736A=	NCBI36
NG_007083.1:g.201364A=
NG_007083.2:g.230820A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11558A= MANE Select	ENSP00000384582.2:p.His3853=
ENST00000425867.3:c.689A=	ENSP00000392618.3:p.His230=
ENST00000639431.1:c.265+78954A=	ENSP00000491057.1:n.265+78954A=
ENST00000640374.1:n.4702A=
ENST00000640464.1:n.1977A=
ENST00000405460.6:c.11558A=	ENSP00000384582.2:p.His3853=
ENST00000509621.1:c.4255A=
NM_032119.3:c.11558A=	NP_115495.3:p.His3853=
NR_003149.1:n.11571A=
XM_011543675.1:c.11555A=	XP_011541977.1:p.His3852=
XM_011543676.1:c.11477A=	XP_011541978.1:p.His3826=
XM_011543677.1:c.8861A=	XP_011541979.1:p.His2954=
XM_011543678.1:c.11558A=	XP_011541980.1:p.His3853=
NM_032119.4:c.11558A= MANE Select	NP_115495.3:p.His3853=
XM_017009963.2:c.11579A=	XP_016865452.1:p.His3860=
XM_017009964.2:c.11576A=	XP_016865453.1:p.His3859=
XM_017009965.1:c.11576A=	XP_016865454.1:p.His3859=
XM_017009966.2:c.11498A=	XP_016865455.1:p.His3833=
XM_017009967.1:c.11483A=	XP_016865456.1:p.His3828=
XM_017009968.2:c.11579A=	XP_016865457.1:p.His3860=
XM_017009969.2:c.11579A=	XP_016865458.1:p.His3860=
XM_017009970.2:c.11579A=	XP_016865459.1:p.His3860=
XM_017009971.2:c.11579A=	XP_016865460.1:p.His3860=
XM_017009972.1:c.4697A=	XP_016865461.1:p.His1566=
XM_017009973.1:c.4676A=	XP_016865462.1:p.His1559=
NR_003149.2:n.11574A=