Canonical Allele Identifier: CA445415700

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90040882C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745065C>A , CM000667.2:g.90745065C>A	GRCh38
NC_000005.9:g.90040882C>A , CM000667.1:g.90040882C>A	GRCh37
NC_000005.8:g.90076638C>A	NCBI36
NG_007083.1:g.191266C>A
NG_007083.2:g.220722C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10569C>A MANE Select	ENSP00000384582.2:p.Gly3523=
ENST00000639431.1:c.265+68856C>A	ENSP00000491057.1:n.265+68856C>A
ENST00000640374.1:n.3713C>A
ENST00000640464.1:n.988C>A
ENST00000405460.6:c.10569C>A	ENSP00000384582.2:p.Gly3523=
ENST00000509621.1:c.3266C>A
NM_032119.3:c.10569C>A	NP_115495.3:p.Gly3523=
NR_003149.1:n.10582C>A
XM_011543675.1:c.10566C>A	XP_011541977.1:p.Gly3522=
XM_011543676.1:c.10488C>A	XP_011541978.1:p.Gly3496=
XM_011543677.1:c.7872C>A	XP_011541979.1:p.Gly2624=
XM_011543678.1:c.10569C>A	XP_011541980.1:p.Gly3523=
XM_011543679.1:c.10569C>A	XP_011541981.1:p.Gly3523=
NM_032119.4:c.10569C>A MANE Select	NP_115495.3:p.Gly3523=
XM_017009963.2:c.10590C>A	XP_016865452.1:p.Gly3530=
XM_017009964.2:c.10587C>A	XP_016865453.1:p.Gly3529=
XM_017009965.1:c.10587C>A	XP_016865454.1:p.Gly3529=
XM_017009966.2:c.10509C>A	XP_016865455.1:p.Gly3503=
XM_017009967.1:c.10494C>A	XP_016865456.1:p.Gly3498=
XM_017009968.2:c.10590C>A	XP_016865457.1:p.Gly3530=
XM_017009969.2:c.10590C>A	XP_016865458.1:p.Gly3530=
XM_017009970.2:c.10590C>A	XP_016865459.1:p.Gly3530=
XM_017009971.2:c.10590C>A	XP_016865460.1:p.Gly3530=
XM_017009972.1:c.3708C>A	XP_016865461.1:p.Gly1236=
XM_017009973.1:c.3687C>A	XP_016865462.1:p.Gly1229=
XM_017009974.2:c.10590C>A	XP_016865463.1:p.Gly3530=
NR_003149.2:n.10585C>A