Canonical Allele Identifier: CA360366799

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050899T>G (hg19) ; chr5:g.90755082T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755082T>G , CM000667.2:g.90755082T>G	GRCh38
NC_000005.9:g.90050899T>G , CM000667.1:g.90050899T>G	GRCh37
NC_000005.8:g.90086655T>G	NCBI36
NG_007083.1:g.201283T>G
NG_007083.2:g.230739T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11477T>G MANE Select	ENSP00000384582.2:p.Val3826Gly
ENST00000425867.3:c.608T>G	ENSP00000392618.3:p.Val203Gly
ENST00000639431.1:c.265+78873T>G	ENSP00000491057.1:n.265+78873T>G
ENST00000640374.1:n.4621T>G
ENST00000640464.1:n.1896T>G
ENST00000405460.6:c.11477T>G	ENSP00000384582.2:p.Val3826Gly
ENST00000509621.1:c.4174T>G
NM_032119.3:c.11477T>G	NP_115495.3:p.Val3826Gly
NR_003149.1:n.11490T>G
XM_011543675.1:c.11474T>G	XP_011541977.1:p.Val3825Gly
XM_011543676.1:c.11396T>G	XP_011541978.1:p.Val3799Gly
XM_011543677.1:c.8780T>G	XP_011541979.1:p.Val2927Gly
XM_011543678.1:c.11477T>G	XP_011541980.1:p.Val3826Gly
NM_032119.4:c.11477T>G MANE Select	NP_115495.3:p.Val3826Gly
XM_017009963.2:c.11498T>G	XP_016865452.1:p.Val3833Gly
XM_017009964.2:c.11495T>G	XP_016865453.1:p.Val3832Gly
XM_017009965.1:c.11495T>G	XP_016865454.1:p.Val3832Gly
XM_017009966.2:c.11417T>G	XP_016865455.1:p.Val3806Gly
XM_017009967.1:c.11402T>G	XP_016865456.1:p.Val3801Gly
XM_017009968.2:c.11498T>G	XP_016865457.1:p.Val3833Gly
XM_017009969.2:c.11498T>G	XP_016865458.1:p.Val3833Gly
XM_017009970.2:c.11498T>G	XP_016865459.1:p.Val3833Gly
XM_017009971.2:c.11498T>G	XP_016865460.1:p.Val3833Gly
XM_017009972.1:c.4616T>G	XP_016865461.1:p.Val1539Gly
XM_017009973.1:c.4595T>G	XP_016865462.1:p.Val1532Gly
NR_003149.2:n.11493T>G