Canonical Allele Identifier: CA360367259

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050974A>G (hg19) ; chr5:g.90755157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755157A>G , CM000667.2:g.90755157A>G	GRCh38
NC_000005.9:g.90050974A>G , CM000667.1:g.90050974A>G	GRCh37
NC_000005.8:g.90086730A>G	NCBI36
NG_007083.1:g.201358A>G
NG_007083.2:g.230814A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11552A>G MANE Select	ENSP00000384582.2:p.Glu3851Gly
ENST00000425867.3:c.683A>G	ENSP00000392618.3:p.Glu228Gly
ENST00000639431.1:c.265+78948A>G	ENSP00000491057.1:n.265+78948A>G
ENST00000640374.1:n.4696A>G
ENST00000640464.1:n.1971A>G
ENST00000405460.6:c.11552A>G	ENSP00000384582.2:p.Glu3851Gly
ENST00000509621.1:c.4249A>G
NM_032119.3:c.11552A>G	NP_115495.3:p.Glu3851Gly
NR_003149.1:n.11565A>G
XM_011543675.1:c.11549A>G	XP_011541977.1:p.Glu3850Gly
XM_011543676.1:c.11471A>G	XP_011541978.1:p.Glu3824Gly
XM_011543677.1:c.8855A>G	XP_011541979.1:p.Glu2952Gly
XM_011543678.1:c.11552A>G	XP_011541980.1:p.Glu3851Gly
NM_032119.4:c.11552A>G MANE Select	NP_115495.3:p.Glu3851Gly
XM_017009963.2:c.11573A>G	XP_016865452.1:p.Glu3858Gly
XM_017009964.2:c.11570A>G	XP_016865453.1:p.Glu3857Gly
XM_017009965.1:c.11570A>G	XP_016865454.1:p.Glu3857Gly
XM_017009966.2:c.11492A>G	XP_016865455.1:p.Glu3831Gly
XM_017009967.1:c.11477A>G	XP_016865456.1:p.Glu3826Gly
XM_017009968.2:c.11573A>G	XP_016865457.1:p.Glu3858Gly
XM_017009969.2:c.11573A>G	XP_016865458.1:p.Glu3858Gly
XM_017009970.2:c.11573A>G	XP_016865459.1:p.Glu3858Gly
XM_017009971.2:c.11573A>G	XP_016865460.1:p.Glu3858Gly
XM_017009972.1:c.4691A>G	XP_016865461.1:p.Glu1564Gly
XM_017009973.1:c.4670A>G	XP_016865462.1:p.Glu1557Gly
NR_003149.2:n.11568A>G