Canonical Allele Identifier: CA445406747

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059214A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763397A>T , CM000667.2:g.90763397A>T	GRCh38
NC_000005.9:g.90059214A>T , CM000667.1:g.90059214A>T	GRCh37
NC_000005.8:g.90094970A>T	NCBI36
NG_007083.1:g.209598A>T
NG_007083.2:g.239054A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12213A>T MANE Select	ENSP00000384582.2:p.Arg4071=
ENST00000425867.3:c.1167A>T	ENSP00000392618.3:p.Arg389=
ENST00000639431.1:c.265+87188A>T	ENSP00000491057.1:n.265+87188A>T
ENST00000640464.1:n.2632A>T
ENST00000640729.1:n.790A>T
ENST00000405460.6:c.12213A>T	ENSP00000384582.2:p.Arg4071=
NM_032119.3:c.12213A>T	NP_115495.3:p.Arg4071=
NR_003149.1:n.12226A>T
XM_011543675.1:c.12210A>T	XP_011541977.1:p.Arg4070=
XM_011543676.1:c.12132A>T	XP_011541978.1:p.Arg4044=
XM_011543677.1:c.9516A>T	XP_011541979.1:p.Arg3172=
XM_011543678.1:c.12213A>T	XP_011541980.1:p.Arg4071=
NM_032119.4:c.12213A>T MANE Select	NP_115495.3:p.Arg4071=
XM_017009963.2:c.12234A>T	XP_016865452.1:p.Arg4078=
XM_017009964.2:c.12231A>T	XP_016865453.1:p.Arg4077=
XM_017009965.1:c.12231A>T	XP_016865454.1:p.Arg4077=
XM_017009966.2:c.12153A>T	XP_016865455.1:p.Arg4051=
XM_017009967.1:c.12138A>T	XP_016865456.1:p.Arg4046=
XM_017009968.2:c.12234A>T	XP_016865457.1:p.Arg4078=
XM_017009969.2:c.12234A>T	XP_016865458.1:p.Arg4078=
XM_017009970.2:c.12234A>T	XP_016865459.1:p.Arg4078=
XM_017009971.2:c.12234A>T	XP_016865460.1:p.Arg4078=
XM_017009972.1:c.5352A>T	XP_016865461.1:p.Arg1784=
XM_017009973.1:c.5331A>T	XP_016865462.1:p.Arg1777=
NR_003149.2:n.12229A>T