Canonical Allele Identifier: CA3340414

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90711275C>G , CM000667.2:g.90711275C>G	GRCh38
NC_000005.9:g.90007092C>G , CM000667.1:g.90007092C>G	GRCh37
NC_000005.8:g.90042848C>G	NCBI36
NG_007083.1:g.157476C>G
NG_007083.2:g.186932C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8995C>G MANE Select	NP_115495.3:p.Gln2999Glu
ENST00000405460.9:c.8995C>G MANE Select	ENSP00000384582.2:p.Gln2999Glu
NM_032119.3:c.8995C>G	NP_115495.3:p.Gln2999Glu
NR_003149.1:n.9008C>G
NR_003149.2:n.9011C>G
ENST00000405460.6:c.8995C>G	ENSP00000384582.2:p.Gln2999Glu
ENST00000509621.1:c.1692C>G
ENST00000639431.1:c.265+35066C>G	ENSP00000491057.1:n.265+35066C>G
ENST00000639473.1:n.4454C>G
ENST00000640012.1:c.2802C>G
ENST00000640374.1:n.2139C>G
ENST00000640779.1:c.3724C>G
XM_011543675.1:c.8992C>G	XP_011541977.1:p.Gln2998Glu
XM_011543676.1:c.8914C>G	XP_011541978.1:p.Gln2972Glu
XM_011543677.1:c.6298C>G	XP_011541979.1:p.Gln2100Glu
XM_011543678.1:c.8995C>G	XP_011541980.1:p.Gln2999Glu
XM_011543679.1:c.8995C>G	XP_011541981.1:p.Gln2999Glu
XM_017009963.2:c.9016C>G	XP_016865452.1:p.Gln3006Glu
XM_017009964.2:c.9013C>G	XP_016865453.1:p.Gln3005Glu
XM_017009965.1:c.9013C>G	XP_016865454.1:p.Gln3005Glu
XM_017009966.2:c.8935C>G	XP_016865455.1:p.Gln2979Glu
XM_017009967.1:c.8920C>G	XP_016865456.1:p.Gln2974Glu
XM_017009968.2:c.9016C>G	XP_016865457.1:p.Gln3006Glu
XM_017009969.2:c.9016C>G	XP_016865458.1:p.Gln3006Glu
XM_017009970.2:c.9016C>G	XP_016865459.1:p.Gln3006Glu
XM_017009971.2:c.9016C>G	XP_016865460.1:p.Gln3006Glu
XM_017009972.1:c.2134C>G	XP_016865461.1:p.Gln712Glu
XM_017009973.1:c.2113C>G	XP_016865462.1:p.Gln705Glu
XM_017009974.2:c.9016C>G	XP_016865463.1:p.Gln3006Glu