Canonical Allele Identifier: CA360366872

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050911C>G (hg19) ; chr5:g.90755094C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755094C>G , CM000667.2:g.90755094C>G	GRCh38
NC_000005.9:g.90050911C>G , CM000667.1:g.90050911C>G	GRCh37
NC_000005.8:g.90086667C>G	NCBI36
NG_007083.1:g.201295C>G
NG_007083.2:g.230751C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11489C>G MANE Select	ENSP00000384582.2:p.Ala3830Gly
ENST00000425867.3:c.620C>G	ENSP00000392618.3:p.Ala207Gly
ENST00000639431.1:c.265+78885C>G	ENSP00000491057.1:n.265+78885C>G
ENST00000640374.1:n.4633C>G
ENST00000640464.1:n.1908C>G
ENST00000405460.6:c.11489C>G	ENSP00000384582.2:p.Ala3830Gly
ENST00000509621.1:c.4186C>G
NM_032119.3:c.11489C>G	NP_115495.3:p.Ala3830Gly
NR_003149.1:n.11502C>G
XM_011543675.1:c.11486C>G	XP_011541977.1:p.Ala3829Gly
XM_011543676.1:c.11408C>G	XP_011541978.1:p.Ala3803Gly
XM_011543677.1:c.8792C>G	XP_011541979.1:p.Ala2931Gly
XM_011543678.1:c.11489C>G	XP_011541980.1:p.Ala3830Gly
NM_032119.4:c.11489C>G MANE Select	NP_115495.3:p.Ala3830Gly
XM_017009963.2:c.11510C>G	XP_016865452.1:p.Ala3837Gly
XM_017009964.2:c.11507C>G	XP_016865453.1:p.Ala3836Gly
XM_017009965.1:c.11507C>G	XP_016865454.1:p.Ala3836Gly
XM_017009966.2:c.11429C>G	XP_016865455.1:p.Ala3810Gly
XM_017009967.1:c.11414C>G	XP_016865456.1:p.Ala3805Gly
XM_017009968.2:c.11510C>G	XP_016865457.1:p.Ala3837Gly
XM_017009969.2:c.11510C>G	XP_016865458.1:p.Ala3837Gly
XM_017009970.2:c.11510C>G	XP_016865459.1:p.Ala3837Gly
XM_017009971.2:c.11510C>G	XP_016865460.1:p.Ala3837Gly
XM_017009972.1:c.4628C>G	XP_016865461.1:p.Ala1543Gly
XM_017009973.1:c.4607C>G	XP_016865462.1:p.Ala1536Gly
NR_003149.2:n.11505C>G