Canonical Allele Identifier: CA360366905

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050917A>C (hg19) ; chr5:g.90755100A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755100A>C , CM000667.2:g.90755100A>C	GRCh38
NC_000005.9:g.90050917A>C , CM000667.1:g.90050917A>C	GRCh37
NC_000005.8:g.90086673A>C	NCBI36
NG_007083.1:g.201301A>C
NG_007083.2:g.230757A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11495A>C MANE Select	ENSP00000384582.2:p.Glu3832Ala
ENST00000425867.3:c.626A>C	ENSP00000392618.3:p.Glu209Ala
ENST00000639431.1:c.265+78891A>C	ENSP00000491057.1:n.265+78891A>C
ENST00000640374.1:n.4639A>C
ENST00000640464.1:n.1914A>C
ENST00000405460.6:c.11495A>C	ENSP00000384582.2:p.Glu3832Ala
ENST00000509621.1:c.4192A>C
NM_032119.3:c.11495A>C	NP_115495.3:p.Glu3832Ala
NR_003149.1:n.11508A>C
XM_011543675.1:c.11492A>C	XP_011541977.1:p.Glu3831Ala
XM_011543676.1:c.11414A>C	XP_011541978.1:p.Glu3805Ala
XM_011543677.1:c.8798A>C	XP_011541979.1:p.Glu2933Ala
XM_011543678.1:c.11495A>C	XP_011541980.1:p.Glu3832Ala
NM_032119.4:c.11495A>C MANE Select	NP_115495.3:p.Glu3832Ala
XM_017009963.2:c.11516A>C	XP_016865452.1:p.Glu3839Ala
XM_017009964.2:c.11513A>C	XP_016865453.1:p.Glu3838Ala
XM_017009965.1:c.11513A>C	XP_016865454.1:p.Glu3838Ala
XM_017009966.2:c.11435A>C	XP_016865455.1:p.Glu3812Ala
XM_017009967.1:c.11420A>C	XP_016865456.1:p.Glu3807Ala
XM_017009968.2:c.11516A>C	XP_016865457.1:p.Glu3839Ala
XM_017009969.2:c.11516A>C	XP_016865458.1:p.Glu3839Ala
XM_017009970.2:c.11516A>C	XP_016865459.1:p.Glu3839Ala
XM_017009971.2:c.11516A>C	XP_016865460.1:p.Glu3839Ala
XM_017009972.1:c.4634A>C	XP_016865461.1:p.Glu1545Ala
XM_017009973.1:c.4613A>C	XP_016865462.1:p.Glu1538Ala
NR_003149.2:n.11511A>C