Canonical Allele Identifier: CA445404465

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988442T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692625T>A , CM000667.2:g.90692625T>A	GRCh38
NC_000005.9:g.89988442T>A , CM000667.1:g.89988442T>A	GRCh37
NC_000005.8:g.90024198T>A	NCBI36
NG_007083.1:g.138826T>A
NG_007083.2:g.168282T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6972T>A MANE Select	ENSP00000384582.2:p.Thr2324=
ENST00000639431.1:c.265+16416T>A	ENSP00000491057.1:n.265+16416T>A
ENST00000639473.1:n.2431T>A
ENST00000640012.1:c.779T>A
ENST00000640374.1:n.116T>A
ENST00000640403.1:c.4263T>A	ENSP00000492531.1:p.Thr1421=
ENST00000640779.1:c.1701T>A
ENST00000405460.6:c.6972T>A	ENSP00000384582.2:p.Thr2324=
NM_032119.3:c.6972T>A	NP_115495.3:p.Thr2324=
NR_003149.1:n.6985T>A
XM_011543675.1:c.6969T>A	XP_011541977.1:p.Thr2323=
XM_011543676.1:c.6891T>A	XP_011541978.1:p.Thr2297=
XM_011543677.1:c.4275T>A	XP_011541979.1:p.Thr1425=
XM_011543678.1:c.6972T>A	XP_011541980.1:p.Thr2324=
XM_011543679.1:c.6972T>A	XP_011541981.1:p.Thr2324=
NM_032119.4:c.6972T>A MANE Select	NP_115495.3:p.Thr2324=
XM_017009963.2:c.6972T>A	XP_016865452.1:p.Thr2324=
XM_017009964.2:c.6969T>A	XP_016865453.1:p.Thr2323=
XM_017009965.1:c.6969T>A	XP_016865454.1:p.Thr2323=
XM_017009966.2:c.6891T>A	XP_016865455.1:p.Thr2297=
XM_017009967.1:c.6876T>A	XP_016865456.1:p.Thr2292=
XM_017009968.2:c.6972T>A	XP_016865457.1:p.Thr2324=
XM_017009969.2:c.6972T>A	XP_016865458.1:p.Thr2324=
XM_017009970.2:c.6972T>A	XP_016865459.1:p.Thr2324=
XM_017009971.2:c.6972T>A	XP_016865460.1:p.Thr2324=
XM_017009972.1:c.90T>A	XP_016865461.1:p.Thr30=
XM_017009973.1:c.90T>A	XP_016865462.1:p.Thr30=
XM_017009974.2:c.6972T>A	XP_016865463.1:p.Thr2324=
NR_003149.2:n.6988T>A