Canonical Allele Identifier: CA445465130

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89923048A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627231A>T , CM000667.2:g.90627231A>T	GRCh38
NC_000005.9:g.89923048A>T , CM000667.1:g.89923048A>T	GRCh37
NC_000005.8:g.89958804A>T	NCBI36
NG_007083.1:g.73432A>T
NG_007083.2:g.102888A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.693A>T MANE Select	ENSP00000384582.2:p.Ile231=
ENST00000640083.1:n.398A>T
ENST00000640109.1:n.789A>T
ENST00000640281.1:n.752A>T
ENST00000405460.6:c.693A>T	ENSP00000384582.2:p.Ile231=
NM_032119.3:c.693A>T	NP_115495.3:p.Ile231=
NR_003149.1:n.789A>T
XM_011543675.1:c.693A>T	XP_011541977.1:p.Ile231=
XM_011543676.1:c.693A>T	XP_011541978.1:p.Ile231=
XM_011543678.1:c.693A>T	XP_011541980.1:p.Ile231=
XM_011543679.1:c.693A>T	XP_011541981.1:p.Ile231=
NM_032119.4:c.693A>T MANE Select	NP_115495.3:p.Ile231=
XM_017009963.2:c.693A>T	XP_016865452.1:p.Ile231=
XM_017009964.2:c.693A>T	XP_016865453.1:p.Ile231=
XM_017009965.1:c.690A>T	XP_016865454.1:p.Ile230=
XM_017009966.2:c.693A>T	XP_016865455.1:p.Ile231=
XM_017009967.1:c.597A>T	XP_016865456.1:p.Ile199=
XM_017009968.2:c.693A>T	XP_016865457.1:p.Ile231=
XM_017009969.2:c.693A>T	XP_016865458.1:p.Ile231=
XM_017009970.2:c.693A>T	XP_016865459.1:p.Ile231=
XM_017009971.2:c.693A>T	XP_016865460.1:p.Ile231=
XM_017009974.2:c.693A>T	XP_016865463.1:p.Ile231=
NR_003149.2:n.792A>T