Canonical Allele Identifier: CA445411767

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008124A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712307A>T , CM000667.2:g.90712307A>T	GRCh38
NC_000005.9:g.90008124A>T , CM000667.1:g.90008124A>T	GRCh37
NC_000005.8:g.90043880A>T	NCBI36
NG_007083.1:g.158508A>T
NG_007083.2:g.187964A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9063A>T MANE Select	ENSP00000384582.2:p.Gly3021=
ENST00000639431.1:c.265+36098A>T	ENSP00000491057.1:n.265+36098A>T
ENST00000639473.1:n.4522A>T
ENST00000640012.1:c.2870A>T
ENST00000640374.1:n.2207A>T
ENST00000640779.1:c.3792A>T
ENST00000405460.6:c.9063A>T	ENSP00000384582.2:p.Gly3021=
ENST00000509621.1:c.1760A>T
NM_032119.3:c.9063A>T	NP_115495.3:p.Gly3021=
NR_003149.1:n.9076A>T
XM_011543675.1:c.9060A>T	XP_011541977.1:p.Gly3020=
XM_011543676.1:c.8982A>T	XP_011541978.1:p.Gly2994=
XM_011543677.1:c.6366A>T	XP_011541979.1:p.Gly2122=
XM_011543678.1:c.9063A>T	XP_011541980.1:p.Gly3021=
XM_011543679.1:c.9063A>T	XP_011541981.1:p.Gly3021=
NM_032119.4:c.9063A>T MANE Select	NP_115495.3:p.Gly3021=
XM_017009963.2:c.9084A>T	XP_016865452.1:p.Gly3028=
XM_017009964.2:c.9081A>T	XP_016865453.1:p.Gly3027=
XM_017009965.1:c.9081A>T	XP_016865454.1:p.Gly3027=
XM_017009966.2:c.9003A>T	XP_016865455.1:p.Gly3001=
XM_017009967.1:c.8988A>T	XP_016865456.1:p.Gly2996=
XM_017009968.2:c.9084A>T	XP_016865457.1:p.Gly3028=
XM_017009969.2:c.9084A>T	XP_016865458.1:p.Gly3028=
XM_017009970.2:c.9084A>T	XP_016865459.1:p.Gly3028=
XM_017009971.2:c.9084A>T	XP_016865460.1:p.Gly3028=
XM_017009972.1:c.2202A>T	XP_016865461.1:p.Gly734=
XM_017009973.1:c.2181A>T	XP_016865462.1:p.Gly727=
XM_017009974.2:c.9084A>T	XP_016865463.1:p.Gly3028=
NR_003149.2:n.9079A>T