Canonical Allele Identifier: CA360366495

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050856A>T (hg19) ; chr5:g.90755039A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755039A>T , CM000667.2:g.90755039A>T	GRCh38
NC_000005.9:g.90050856A>T , CM000667.1:g.90050856A>T	GRCh37
NC_000005.8:g.90086612A>T	NCBI36
NG_007083.1:g.201240A>T
NG_007083.2:g.230696A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11434A>T MANE Select	ENSP00000384582.2:p.Ile3812Phe
ENST00000425867.3:c.565A>T	ENSP00000392618.3:p.Ile189Phe
ENST00000639431.1:c.265+78830A>T	ENSP00000491057.1:n.265+78830A>T
ENST00000640374.1:n.4578A>T
ENST00000640464.1:n.1853A>T
ENST00000405460.6:c.11434A>T	ENSP00000384582.2:p.Ile3812Phe
ENST00000509621.1:c.4131A>T
NM_032119.3:c.11434A>T	NP_115495.3:p.Ile3812Phe
NR_003149.1:n.11447A>T
XM_011543675.1:c.11431A>T	XP_011541977.1:p.Ile3811Phe
XM_011543676.1:c.11353A>T	XP_011541978.1:p.Ile3785Phe
XM_011543677.1:c.8737A>T	XP_011541979.1:p.Ile2913Phe
XM_011543678.1:c.11434A>T	XP_011541980.1:p.Ile3812Phe
NM_032119.4:c.11434A>T MANE Select	NP_115495.3:p.Ile3812Phe
XM_017009963.2:c.11455A>T	XP_016865452.1:p.Ile3819Phe
XM_017009964.2:c.11452A>T	XP_016865453.1:p.Ile3818Phe
XM_017009965.1:c.11452A>T	XP_016865454.1:p.Ile3818Phe
XM_017009966.2:c.11374A>T	XP_016865455.1:p.Ile3792Phe
XM_017009967.1:c.11359A>T	XP_016865456.1:p.Ile3787Phe
XM_017009968.2:c.11455A>T	XP_016865457.1:p.Ile3819Phe
XM_017009969.2:c.11455A>T	XP_016865458.1:p.Ile3819Phe
XM_017009970.2:c.11455A>T	XP_016865459.1:p.Ile3819Phe
XM_017009971.2:c.11455A>T	XP_016865460.1:p.Ile3819Phe
XM_017009972.1:c.4573A>T	XP_016865461.1:p.Ile1525Phe
XM_017009973.1:c.4552A>T	XP_016865462.1:p.Ile1518Phe
NR_003149.2:n.11450A>T