Canonical Allele Identifier: CA360367044

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050937C>G (hg19) ; chr5:g.90755120C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755120C>G , CM000667.2:g.90755120C>G	GRCh38
NC_000005.9:g.90050937C>G , CM000667.1:g.90050937C>G	GRCh37
NC_000005.8:g.90086693C>G	NCBI36
NG_007083.1:g.201321C>G
NG_007083.2:g.230777C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11515C>G MANE Select	ENSP00000384582.2:p.Gln3839Glu
ENST00000425867.3:c.646C>G	ENSP00000392618.3:p.Gln216Glu
ENST00000639431.1:c.265+78911C>G	ENSP00000491057.1:n.265+78911C>G
ENST00000640374.1:n.4659C>G
ENST00000640464.1:n.1934C>G
ENST00000405460.6:c.11515C>G	ENSP00000384582.2:p.Gln3839Glu
ENST00000509621.1:c.4212C>G
NM_032119.3:c.11515C>G	NP_115495.3:p.Gln3839Glu
NR_003149.1:n.11528C>G
XM_011543675.1:c.11512C>G	XP_011541977.1:p.Gln3838Glu
XM_011543676.1:c.11434C>G	XP_011541978.1:p.Gln3812Glu
XM_011543677.1:c.8818C>G	XP_011541979.1:p.Gln2940Glu
XM_011543678.1:c.11515C>G	XP_011541980.1:p.Gln3839Glu
NM_032119.4:c.11515C>G MANE Select	NP_115495.3:p.Gln3839Glu
XM_017009963.2:c.11536C>G	XP_016865452.1:p.Gln3846Glu
XM_017009964.2:c.11533C>G	XP_016865453.1:p.Gln3845Glu
XM_017009965.1:c.11533C>G	XP_016865454.1:p.Gln3845Glu
XM_017009966.2:c.11455C>G	XP_016865455.1:p.Gln3819Glu
XM_017009967.1:c.11440C>G	XP_016865456.1:p.Gln3814Glu
XM_017009968.2:c.11536C>G	XP_016865457.1:p.Gln3846Glu
XM_017009969.2:c.11536C>G	XP_016865458.1:p.Gln3846Glu
XM_017009970.2:c.11536C>G	XP_016865459.1:p.Gln3846Glu
XM_017009971.2:c.11536C>G	XP_016865460.1:p.Gln3846Glu
XM_017009972.1:c.4654C>G	XP_016865461.1:p.Gln1552Glu
XM_017009973.1:c.4633C>G	XP_016865462.1:p.Gln1545Glu
NR_003149.2:n.11531C>G