Canonical Allele Identifier: CA360366901

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050916G>C (hg19) ; chr5:g.90755099G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755099G>C , CM000667.2:g.90755099G>C	GRCh38
NC_000005.9:g.90050916G>C , CM000667.1:g.90050916G>C	GRCh37
NC_000005.8:g.90086672G>C	NCBI36
NG_007083.1:g.201300G>C
NG_007083.2:g.230756G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11494G>C MANE Select	ENSP00000384582.2:p.Glu3832Gln
ENST00000425867.3:c.625G>C	ENSP00000392618.3:p.Glu209Gln
ENST00000639431.1:c.265+78890G>C	ENSP00000491057.1:n.265+78890G>C
ENST00000640374.1:n.4638G>C
ENST00000640464.1:n.1913G>C
ENST00000405460.6:c.11494G>C	ENSP00000384582.2:p.Glu3832Gln
ENST00000509621.1:c.4191G>C
NM_032119.3:c.11494G>C	NP_115495.3:p.Glu3832Gln
NR_003149.1:n.11507G>C
XM_011543675.1:c.11491G>C	XP_011541977.1:p.Glu3831Gln
XM_011543676.1:c.11413G>C	XP_011541978.1:p.Glu3805Gln
XM_011543677.1:c.8797G>C	XP_011541979.1:p.Glu2933Gln
XM_011543678.1:c.11494G>C	XP_011541980.1:p.Glu3832Gln
NM_032119.4:c.11494G>C MANE Select	NP_115495.3:p.Glu3832Gln
XM_017009963.2:c.11515G>C	XP_016865452.1:p.Glu3839Gln
XM_017009964.2:c.11512G>C	XP_016865453.1:p.Glu3838Gln
XM_017009965.1:c.11512G>C	XP_016865454.1:p.Glu3838Gln
XM_017009966.2:c.11434G>C	XP_016865455.1:p.Glu3812Gln
XM_017009967.1:c.11419G>C	XP_016865456.1:p.Glu3807Gln
XM_017009968.2:c.11515G>C	XP_016865457.1:p.Glu3839Gln
XM_017009969.2:c.11515G>C	XP_016865458.1:p.Glu3839Gln
XM_017009970.2:c.11515G>C	XP_016865459.1:p.Glu3839Gln
XM_017009971.2:c.11515G>C	XP_016865460.1:p.Glu3839Gln
XM_017009972.1:c.4633G>C	XP_016865461.1:p.Glu1545Gln
XM_017009973.1:c.4612G>C	XP_016865462.1:p.Glu1538Gln
NR_003149.2:n.11510G>C