Canonical Allele Identifier: CA445404161

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050948A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755131A>T , CM000667.2:g.90755131A>T	GRCh38
NC_000005.9:g.90050948A>T , CM000667.1:g.90050948A>T	GRCh37
NC_000005.8:g.90086704A>T	NCBI36
NG_007083.1:g.201332A>T
NG_007083.2:g.230788A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11526A>T MANE Select	ENSP00000384582.2:p.Ile3842=
ENST00000425867.3:c.657A>T	ENSP00000392618.3:p.Ile219=
ENST00000639431.1:c.265+78922A>T	ENSP00000491057.1:n.265+78922A>T
ENST00000640374.1:n.4670A>T
ENST00000640464.1:n.1945A>T
ENST00000405460.6:c.11526A>T	ENSP00000384582.2:p.Ile3842=
ENST00000509621.1:c.4223A>T
NM_032119.3:c.11526A>T	NP_115495.3:p.Ile3842=
NR_003149.1:n.11539A>T
XM_011543675.1:c.11523A>T	XP_011541977.1:p.Ile3841=
XM_011543676.1:c.11445A>T	XP_011541978.1:p.Ile3815=
XM_011543677.1:c.8829A>T	XP_011541979.1:p.Ile2943=
XM_011543678.1:c.11526A>T	XP_011541980.1:p.Ile3842=
NM_032119.4:c.11526A>T MANE Select	NP_115495.3:p.Ile3842=
XM_017009963.2:c.11547A>T	XP_016865452.1:p.Ile3849=
XM_017009964.2:c.11544A>T	XP_016865453.1:p.Ile3848=
XM_017009965.1:c.11544A>T	XP_016865454.1:p.Ile3848=
XM_017009966.2:c.11466A>T	XP_016865455.1:p.Ile3822=
XM_017009967.1:c.11451A>T	XP_016865456.1:p.Ile3817=
XM_017009968.2:c.11547A>T	XP_016865457.1:p.Ile3849=
XM_017009969.2:c.11547A>T	XP_016865458.1:p.Ile3849=
XM_017009970.2:c.11547A>T	XP_016865459.1:p.Ile3849=
XM_017009971.2:c.11547A>T	XP_016865460.1:p.Ile3849=
XM_017009972.1:c.4665A>T	XP_016865461.1:p.Ile1555=
XM_017009973.1:c.4644A>T	XP_016865462.1:p.Ile1548=
NR_003149.2:n.11542A>T