Canonical Allele Identifier: CA3341513

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90783303T>G , CM000667.2:g.90783303T>G	GRCh38
NC_000005.9:g.90079120T>G , CM000667.1:g.90079120T>G	GRCh37
NC_000005.8:g.90114876T>G	NCBI36
NG_007083.1:g.229504T>G
NG_007083.2:g.258960T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13411T>G MANE Select	NP_115495.3:p.Ser4471Ala
ENST00000405460.9:c.13411T>G MANE Select	ENSP00000384582.2:p.Ser4471Ala
NM_032119.3:c.13411T>G	NP_115495.3:p.Ser4471Ala
NR_003149.1:n.13424T>G
NR_003149.2:n.13427T>G
ENST00000405460.6:c.13411T>G	ENSP00000384582.2:p.Ser4471Ala
ENST00000425867.2:c.394T>G	ENSP00000392618.2:p.Ser132Ala
ENST00000425867.3:c.2365T>G	ENSP00000392618.3:p.Ser789Ala
ENST00000638510.1:n.678T>G
ENST00000638975.1:c.40T>G	ENSP00000492630.1:p.Ser14Ala
ENST00000639431.1:c.265+107094T>G	ENSP00000491057.1:n.265+107094T>G
XM_011543675.1:c.13408T>G	XP_011541977.1:p.Ser4470Ala
XM_011543676.1:c.13330T>G	XP_011541978.1:p.Ser4444Ala
XM_011543677.1:c.10714T>G	XP_011541979.1:p.Ser3572Ala
XM_011543678.1:c.13411T>G	XP_011541980.1:p.Ser4471Ala
XM_017009963.2:c.13432T>G	XP_016865452.1:p.Ser4478Ala
XM_017009964.2:c.13429T>G	XP_016865453.1:p.Ser4477Ala
XM_017009965.1:c.13429T>G	XP_016865454.1:p.Ser4477Ala
XM_017009966.2:c.13351T>G	XP_016865455.1:p.Ser4451Ala
XM_017009967.1:c.13336T>G	XP_016865456.1:p.Ser4446Ala
XM_017009968.2:c.13432T>G	XP_016865457.1:p.Ser4478Ala
XM_017009969.2:c.13432T>G	XP_016865458.1:p.Ser4478Ala
XM_017009970.2:c.13432T>G	XP_016865459.1:p.Ser4478Ala
XM_017009971.2:c.13432T>G	XP_016865460.1:p.Ser4478Ala
XM_017009972.1:c.6550T>G	XP_016865461.1:p.Ser2184Ala
XM_017009973.1:c.6529T>G	XP_016865462.1:p.Ser2177Ala