Canonical Allele Identifier: CA445412083

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008220A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712403A>T , CM000667.2:g.90712403A>T	GRCh38
NC_000005.9:g.90008220A>T , CM000667.1:g.90008220A>T	GRCh37
NC_000005.8:g.90043976A>T	NCBI36
NG_007083.1:g.158604A>T
NG_007083.2:g.188060A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9159A>T MANE Select	ENSP00000384582.2:p.Gly3053=
ENST00000639431.1:c.265+36194A>T	ENSP00000491057.1:n.265+36194A>T
ENST00000639473.1:n.4618A>T
ENST00000640012.1:c.2966A>T
ENST00000640374.1:n.2303A>T
ENST00000640779.1:c.3888A>T
ENST00000405460.6:c.9159A>T	ENSP00000384582.2:p.Gly3053=
ENST00000509621.1:c.1856A>T
NM_032119.3:c.9159A>T	NP_115495.3:p.Gly3053=
NR_003149.1:n.9172A>T
XM_011543675.1:c.9156A>T	XP_011541977.1:p.Gly3052=
XM_011543676.1:c.9078A>T	XP_011541978.1:p.Gly3026=
XM_011543677.1:c.6462A>T	XP_011541979.1:p.Gly2154=
XM_011543678.1:c.9159A>T	XP_011541980.1:p.Gly3053=
XM_011543679.1:c.9159A>T	XP_011541981.1:p.Gly3053=
XR_948560.1:n.443T>A
NM_032119.4:c.9159A>T MANE Select	NP_115495.3:p.Gly3053=
XM_017009963.2:c.9180A>T	XP_016865452.1:p.Gly3060=
XM_017009964.2:c.9177A>T	XP_016865453.1:p.Gly3059=
XM_017009965.1:c.9177A>T	XP_016865454.1:p.Gly3059=
XM_017009966.2:c.9099A>T	XP_016865455.1:p.Gly3033=
XM_017009967.1:c.9084A>T	XP_016865456.1:p.Gly3028=
XM_017009968.2:c.9180A>T	XP_016865457.1:p.Gly3060=
XM_017009969.2:c.9180A>T	XP_016865458.1:p.Gly3060=
XM_017009970.2:c.9180A>T	XP_016865459.1:p.Gly3060=
XM_017009971.2:c.9180A>T	XP_016865460.1:p.Gly3060=
XM_017009972.1:c.2298A>T	XP_016865461.1:p.Gly766=
XM_017009973.1:c.2277A>T	XP_016865462.1:p.Gly759=
XM_017009974.2:c.9180A>T	XP_016865463.1:p.Gly3060=
NR_003149.2:n.9175A>T