Canonical Allele Identifier: CA445404194

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050969A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755152A>C , CM000667.2:g.90755152A>C	GRCh38
NC_000005.9:g.90050969A>C , CM000667.1:g.90050969A>C	GRCh37
NC_000005.8:g.90086725A>C	NCBI36
NG_007083.1:g.201353A>C
NG_007083.2:g.230809A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11547A>C MANE Select	ENSP00000384582.2:p.Ile3849=
ENST00000425867.3:c.678A>C	ENSP00000392618.3:p.Ile226=
ENST00000639431.1:c.265+78943A>C	ENSP00000491057.1:n.265+78943A>C
ENST00000640374.1:n.4691A>C
ENST00000640464.1:n.1966A>C
ENST00000405460.6:c.11547A>C	ENSP00000384582.2:p.Ile3849=
ENST00000509621.1:c.4244A>C
NM_032119.3:c.11547A>C	NP_115495.3:p.Ile3849=
NR_003149.1:n.11560A>C
XM_011543675.1:c.11544A>C	XP_011541977.1:p.Ile3848=
XM_011543676.1:c.11466A>C	XP_011541978.1:p.Ile3822=
XM_011543677.1:c.8850A>C	XP_011541979.1:p.Ile2950=
XM_011543678.1:c.11547A>C	XP_011541980.1:p.Ile3849=
NM_032119.4:c.11547A>C MANE Select	NP_115495.3:p.Ile3849=
XM_017009963.2:c.11568A>C	XP_016865452.1:p.Ile3856=
XM_017009964.2:c.11565A>C	XP_016865453.1:p.Ile3855=
XM_017009965.1:c.11565A>C	XP_016865454.1:p.Ile3855=
XM_017009966.2:c.11487A>C	XP_016865455.1:p.Ile3829=
XM_017009967.1:c.11472A>C	XP_016865456.1:p.Ile3824=
XM_017009968.2:c.11568A>C	XP_016865457.1:p.Ile3856=
XM_017009969.2:c.11568A>C	XP_016865458.1:p.Ile3856=
XM_017009970.2:c.11568A>C	XP_016865459.1:p.Ile3856=
XM_017009971.2:c.11568A>C	XP_016865460.1:p.Ile3856=
XM_017009972.1:c.4686A>C	XP_016865461.1:p.Ile1562=
XM_017009973.1:c.4665A>C	XP_016865462.1:p.Ile1555=
NR_003149.2:n.11563A>C