Canonical Allele Identifier: CA360366914

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050918G>C (hg19) ; chr5:g.90755101G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755101G>C , CM000667.2:g.90755101G>C	GRCh38
NC_000005.9:g.90050918G>C , CM000667.1:g.90050918G>C	GRCh37
NC_000005.8:g.90086674G>C	NCBI36
NG_007083.1:g.201302G>C
NG_007083.2:g.230758G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11496G>C MANE Select	ENSP00000384582.2:p.Glu3832Asp
ENST00000425867.3:c.627G>C	ENSP00000392618.3:p.Glu209Asp
ENST00000639431.1:c.265+78892G>C	ENSP00000491057.1:n.265+78892G>C
ENST00000640374.1:n.4640G>C
ENST00000640464.1:n.1915G>C
ENST00000405460.6:c.11496G>C	ENSP00000384582.2:p.Glu3832Asp
ENST00000509621.1:c.4193G>C
NM_032119.3:c.11496G>C	NP_115495.3:p.Glu3832Asp
NR_003149.1:n.11509G>C
XM_011543675.1:c.11493G>C	XP_011541977.1:p.Glu3831Asp
XM_011543676.1:c.11415G>C	XP_011541978.1:p.Glu3805Asp
XM_011543677.1:c.8799G>C	XP_011541979.1:p.Glu2933Asp
XM_011543678.1:c.11496G>C	XP_011541980.1:p.Glu3832Asp
NM_032119.4:c.11496G>C MANE Select	NP_115495.3:p.Glu3832Asp
XM_017009963.2:c.11517G>C	XP_016865452.1:p.Glu3839Asp
XM_017009964.2:c.11514G>C	XP_016865453.1:p.Glu3838Asp
XM_017009965.1:c.11514G>C	XP_016865454.1:p.Glu3838Asp
XM_017009966.2:c.11436G>C	XP_016865455.1:p.Glu3812Asp
XM_017009967.1:c.11421G>C	XP_016865456.1:p.Glu3807Asp
XM_017009968.2:c.11517G>C	XP_016865457.1:p.Glu3839Asp
XM_017009969.2:c.11517G>C	XP_016865458.1:p.Glu3839Asp
XM_017009970.2:c.11517G>C	XP_016865459.1:p.Glu3839Asp
XM_017009971.2:c.11517G>C	XP_016865460.1:p.Glu3839Asp
XM_017009972.1:c.4635G>C	XP_016865461.1:p.Glu1545Asp
XM_017009973.1:c.4614G>C	XP_016865462.1:p.Glu1538Asp
NR_003149.2:n.11512G>C