Canonical Allele Identifier: CA360378157

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059219A>G (hg19) ; chr5:g.90763402A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763402A>G , CM000667.2:g.90763402A>G	GRCh38
NC_000005.9:g.90059219A>G , CM000667.1:g.90059219A>G	GRCh37
NC_000005.8:g.90094975A>G	NCBI36
NG_007083.1:g.209603A>G
NG_007083.2:g.239059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12218A>G MANE Select	ENSP00000384582.2:p.Glu4073Gly
ENST00000425867.3:c.1172A>G	ENSP00000392618.3:p.Glu391Gly
ENST00000639431.1:c.265+87193A>G	ENSP00000491057.1:n.265+87193A>G
ENST00000640464.1:n.2637A>G
ENST00000640729.1:n.795A>G
ENST00000405460.6:c.12218A>G	ENSP00000384582.2:p.Glu4073Gly
NM_032119.3:c.12218A>G	NP_115495.3:p.Glu4073Gly
NR_003149.1:n.12231A>G
XM_011543675.1:c.12215A>G	XP_011541977.1:p.Glu4072Gly
XM_011543676.1:c.12137A>G	XP_011541978.1:p.Glu4046Gly
XM_011543677.1:c.9521A>G	XP_011541979.1:p.Glu3174Gly
XM_011543678.1:c.12218A>G	XP_011541980.1:p.Glu4073Gly
NM_032119.4:c.12218A>G MANE Select	NP_115495.3:p.Glu4073Gly
XM_017009963.2:c.12239A>G	XP_016865452.1:p.Glu4080Gly
XM_017009964.2:c.12236A>G	XP_016865453.1:p.Glu4079Gly
XM_017009965.1:c.12236A>G	XP_016865454.1:p.Glu4079Gly
XM_017009966.2:c.12158A>G	XP_016865455.1:p.Glu4053Gly
XM_017009967.1:c.12143A>G	XP_016865456.1:p.Glu4048Gly
XM_017009968.2:c.12239A>G	XP_016865457.1:p.Glu4080Gly
XM_017009969.2:c.12239A>G	XP_016865458.1:p.Glu4080Gly
XM_017009970.2:c.12239A>G	XP_016865459.1:p.Glu4080Gly
XM_017009971.2:c.12239A>G	XP_016865460.1:p.Glu4080Gly
XM_017009972.1:c.5357A>G	XP_016865461.1:p.Glu1786Gly
XM_017009973.1:c.5336A>G	XP_016865462.1:p.Glu1779Gly
NR_003149.2:n.12234A>G