Canonical Allele Identifier: CA445404106

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050915T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755098T>A , CM000667.2:g.90755098T>A	GRCh38
NC_000005.9:g.90050915T>A , CM000667.1:g.90050915T>A	GRCh37
NC_000005.8:g.90086671T>A	NCBI36
NG_007083.1:g.201299T>A
NG_007083.2:g.230755T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11493T>A MANE Select	ENSP00000384582.2:p.Thr3831=
ENST00000425867.3:c.624T>A	ENSP00000392618.3:p.Thr208=
ENST00000639431.1:c.265+78889T>A	ENSP00000491057.1:n.265+78889T>A
ENST00000640374.1:n.4637T>A
ENST00000640464.1:n.1912T>A
ENST00000405460.6:c.11493T>A	ENSP00000384582.2:p.Thr3831=
ENST00000509621.1:c.4190T>A
NM_032119.3:c.11493T>A	NP_115495.3:p.Thr3831=
NR_003149.1:n.11506T>A
XM_011543675.1:c.11490T>A	XP_011541977.1:p.Thr3830=
XM_011543676.1:c.11412T>A	XP_011541978.1:p.Thr3804=
XM_011543677.1:c.8796T>A	XP_011541979.1:p.Thr2932=
XM_011543678.1:c.11493T>A	XP_011541980.1:p.Thr3831=
NM_032119.4:c.11493T>A MANE Select	NP_115495.3:p.Thr3831=
XM_017009963.2:c.11514T>A	XP_016865452.1:p.Thr3838=
XM_017009964.2:c.11511T>A	XP_016865453.1:p.Thr3837=
XM_017009965.1:c.11511T>A	XP_016865454.1:p.Thr3837=
XM_017009966.2:c.11433T>A	XP_016865455.1:p.Thr3811=
XM_017009967.1:c.11418T>A	XP_016865456.1:p.Thr3806=
XM_017009968.2:c.11514T>A	XP_016865457.1:p.Thr3838=
XM_017009969.2:c.11514T>A	XP_016865458.1:p.Thr3838=
XM_017009970.2:c.11514T>A	XP_016865459.1:p.Thr3838=
XM_017009971.2:c.11514T>A	XP_016865460.1:p.Thr3838=
XM_017009972.1:c.4632T>A	XP_016865461.1:p.Thr1544=
XM_017009973.1:c.4611T>A	XP_016865462.1:p.Thr1537=
NR_003149.2:n.11509T>A