Canonical Allele Identifier: CA445411998

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008199T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712382T>A , CM000667.2:g.90712382T>A	GRCh38
NC_000005.9:g.90008199T>A , CM000667.1:g.90008199T>A	GRCh37
NC_000005.8:g.90043955T>A	NCBI36
NG_007083.1:g.158583T>A
NG_007083.2:g.188039T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9138T>A MANE Select	ENSP00000384582.2:p.Ile3046=
ENST00000639431.1:c.265+36173T>A	ENSP00000491057.1:n.265+36173T>A
ENST00000639473.1:n.4597T>A
ENST00000640012.1:c.2945T>A
ENST00000640374.1:n.2282T>A
ENST00000640779.1:c.3867T>A
ENST00000405460.6:c.9138T>A	ENSP00000384582.2:p.Ile3046=
ENST00000509621.1:c.1835T>A
NM_032119.3:c.9138T>A	NP_115495.3:p.Ile3046=
NR_003149.1:n.9151T>A
XM_011543675.1:c.9135T>A	XP_011541977.1:p.Ile3045=
XM_011543676.1:c.9057T>A	XP_011541978.1:p.Ile3019=
XM_011543677.1:c.6441T>A	XP_011541979.1:p.Ile2147=
XM_011543678.1:c.9138T>A	XP_011541980.1:p.Ile3046=
XM_011543679.1:c.9138T>A	XP_011541981.1:p.Ile3046=
XR_948560.1:n.464A>T
NM_032119.4:c.9138T>A MANE Select	NP_115495.3:p.Ile3046=
XM_017009963.2:c.9159T>A	XP_016865452.1:p.Ile3053=
XM_017009964.2:c.9156T>A	XP_016865453.1:p.Ile3052=
XM_017009965.1:c.9156T>A	XP_016865454.1:p.Ile3052=
XM_017009966.2:c.9078T>A	XP_016865455.1:p.Ile3026=
XM_017009967.1:c.9063T>A	XP_016865456.1:p.Ile3021=
XM_017009968.2:c.9159T>A	XP_016865457.1:p.Ile3053=
XM_017009969.2:c.9159T>A	XP_016865458.1:p.Ile3053=
XM_017009970.2:c.9159T>A	XP_016865459.1:p.Ile3053=
XM_017009971.2:c.9159T>A	XP_016865460.1:p.Ile3053=
XM_017009972.1:c.2277T>A	XP_016865461.1:p.Ile759=
XM_017009973.1:c.2256T>A	XP_016865462.1:p.Ile752=
XM_017009974.2:c.9159T>A	XP_016865463.1:p.Ile3053=
NR_003149.2:n.9154T>A