Canonical Allele Identifier: CA445404105

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050912T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755095T>G , CM000667.2:g.90755095T>G	GRCh38
NC_000005.9:g.90050912T>G , CM000667.1:g.90050912T>G	GRCh37
NC_000005.8:g.90086668T>G	NCBI36
NG_007083.1:g.201296T>G
NG_007083.2:g.230752T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11490T>G MANE Select	ENSP00000384582.2:p.Ala3830=
ENST00000425867.3:c.621T>G	ENSP00000392618.3:p.Ala207=
ENST00000639431.1:c.265+78886T>G	ENSP00000491057.1:n.265+78886T>G
ENST00000640374.1:n.4634T>G
ENST00000640464.1:n.1909T>G
ENST00000405460.6:c.11490T>G	ENSP00000384582.2:p.Ala3830=
ENST00000509621.1:c.4187T>G
NM_032119.3:c.11490T>G	NP_115495.3:p.Ala3830=
NR_003149.1:n.11503T>G
XM_011543675.1:c.11487T>G	XP_011541977.1:p.Ala3829=
XM_011543676.1:c.11409T>G	XP_011541978.1:p.Ala3803=
XM_011543677.1:c.8793T>G	XP_011541979.1:p.Ala2931=
XM_011543678.1:c.11490T>G	XP_011541980.1:p.Ala3830=
NM_032119.4:c.11490T>G MANE Select	NP_115495.3:p.Ala3830=
XM_017009963.2:c.11511T>G	XP_016865452.1:p.Ala3837=
XM_017009964.2:c.11508T>G	XP_016865453.1:p.Ala3836=
XM_017009965.1:c.11508T>G	XP_016865454.1:p.Ala3836=
XM_017009966.2:c.11430T>G	XP_016865455.1:p.Ala3810=
XM_017009967.1:c.11415T>G	XP_016865456.1:p.Ala3805=
XM_017009968.2:c.11511T>G	XP_016865457.1:p.Ala3837=
XM_017009969.2:c.11511T>G	XP_016865458.1:p.Ala3837=
XM_017009970.2:c.11511T>G	XP_016865459.1:p.Ala3837=
XM_017009971.2:c.11511T>G	XP_016865460.1:p.Ala3837=
XM_017009972.1:c.4629T>G	XP_016865461.1:p.Ala1543=
XM_017009973.1:c.4608T>G	XP_016865462.1:p.Ala1536=
NR_003149.2:n.11506T>G