Canonical Allele Identifier: CA445413980

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012519T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716702T>A , CM000667.2:g.90716702T>A	GRCh38
NC_000005.9:g.90012519T>A , CM000667.1:g.90012519T>A	GRCh37
NC_000005.8:g.90048275T>A	NCBI36
NG_007083.1:g.162903T>A
NG_007083.2:g.192359T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9420T>A MANE Select	ENSP00000384582.2:p.Ile3140=
ENST00000639431.1:c.265+40493T>A	ENSP00000491057.1:n.265+40493T>A
ENST00000639473.1:n.4879T>A
ENST00000640012.1:c.3227T>A
ENST00000640374.1:n.2564T>A
ENST00000640779.1:c.4149T>A
ENST00000405460.6:c.9420T>A	ENSP00000384582.2:p.Ile3140=
ENST00000509621.1:c.2117T>A
NM_032119.3:c.9420T>A	NP_115495.3:p.Ile3140=
NR_003149.1:n.9433T>A
XM_011543675.1:c.9417T>A	XP_011541977.1:p.Ile3139=
XM_011543676.1:c.9339T>A	XP_011541978.1:p.Ile3113=
XM_011543677.1:c.6723T>A	XP_011541979.1:p.Ile2241=
XM_011543678.1:c.9420T>A	XP_011541980.1:p.Ile3140=
XM_011543679.1:c.9420T>A	XP_011541981.1:p.Ile3140=
XR_948560.1:n.272-893A>T
NM_032119.4:c.9420T>A MANE Select	NP_115495.3:p.Ile3140=
XM_017009963.2:c.9441T>A	XP_016865452.1:p.Ile3147=
XM_017009964.2:c.9438T>A	XP_016865453.1:p.Ile3146=
XM_017009965.1:c.9438T>A	XP_016865454.1:p.Ile3146=
XM_017009966.2:c.9360T>A	XP_016865455.1:p.Ile3120=
XM_017009967.1:c.9345T>A	XP_016865456.1:p.Ile3115=
XM_017009968.2:c.9441T>A	XP_016865457.1:p.Ile3147=
XM_017009969.2:c.9441T>A	XP_016865458.1:p.Ile3147=
XM_017009970.2:c.9441T>A	XP_016865459.1:p.Ile3147=
XM_017009971.2:c.9441T>A	XP_016865460.1:p.Ile3147=
XM_017009972.1:c.2559T>A	XP_016865461.1:p.Ile853=
XM_017009973.1:c.2538T>A	XP_016865462.1:p.Ile846=
XM_017009974.2:c.9441T>A	XP_016865463.1:p.Ile3147=
XR_001742802.1:n.2523-893A>T
NR_003149.2:n.9436T>A