Canonical Allele Identifier: CA445416028

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041423A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745606A>C , CM000667.2:g.90745606A>C	GRCh38
NC_000005.9:g.90041423A>C , CM000667.1:g.90041423A>C	GRCh37
NC_000005.8:g.90077179A>C	NCBI36
NG_007083.1:g.191807A>C
NG_007083.2:g.221263A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10785A>C MANE Select	ENSP00000384582.2:p.Ile3595=
ENST00000639431.1:c.265+69397A>C	ENSP00000491057.1:n.265+69397A>C
ENST00000640374.1:n.3929A>C
ENST00000640464.1:n.1204A>C
ENST00000405460.6:c.10785A>C	ENSP00000384582.2:p.Ile3595=
ENST00000509621.1:c.3482A>C
NM_032119.3:c.10785A>C	NP_115495.3:p.Ile3595=
NR_003149.1:n.10798A>C
XM_011543675.1:c.10782A>C	XP_011541977.1:p.Ile3594=
XM_011543676.1:c.10704A>C	XP_011541978.1:p.Ile3568=
XM_011543677.1:c.8088A>C	XP_011541979.1:p.Ile2696=
XM_011543678.1:c.10785A>C	XP_011541980.1:p.Ile3595=
XM_011543679.1:c.*7A>C	XP_011541981.1:n.*7A>C
NM_032119.4:c.10785A>C MANE Select	NP_115495.3:p.Ile3595=
XM_017009963.2:c.10806A>C	XP_016865452.1:p.Ile3602=
XM_017009964.2:c.10803A>C	XP_016865453.1:p.Ile3601=
XM_017009965.1:c.10803A>C	XP_016865454.1:p.Ile3601=
XM_017009966.2:c.10725A>C	XP_016865455.1:p.Ile3575=
XM_017009967.1:c.10710A>C	XP_016865456.1:p.Ile3570=
XM_017009968.2:c.10806A>C	XP_016865457.1:p.Ile3602=
XM_017009969.2:c.10806A>C	XP_016865458.1:p.Ile3602=
XM_017009970.2:c.10806A>C	XP_016865459.1:p.Ile3602=
XM_017009971.2:c.10806A>C	XP_016865460.1:p.Ile3602=
XM_017009972.1:c.3924A>C	XP_016865461.1:p.Ile1308=
XM_017009973.1:c.3903A>C	XP_016865462.1:p.Ile1301=
XM_017009974.2:c.*7A>C	XP_016865463.1:n.*7A>C
NR_003149.2:n.10801A>C