Canonical Allele Identifier: CA121841180

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90657967C>T , CM000667.2:g.90657967C>T	GRCh38
NC_000005.9:g.89953784C>T , CM000667.1:g.89953784C>T	GRCh37
NC_000005.8:g.89989540C>T	NCBI36
NG_007083.1:g.104168C>T
NG_007083.2:g.133624C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.4441C>T MANE Select	NP_115495.3:p.Gln1481Ter
ENST00000405460.9:c.4441C>T MANE Select	ENSP00000384582.2:p.Gln1481Ter
NM_032119.3:c.4441C>T	NP_115495.3:p.Gln1481Ter
NR_003149.1:n.4537C>T
NR_003149.2:n.4540C>T
ENST00000405460.6:c.4441C>T	ENSP00000384582.2:p.Gln1481Ter
ENST00000639676.1:n.2039C>T
ENST00000640403.1:c.1732C>T	ENSP00000492531.1:p.Gln578Ter
XM_011543675.1:c.4441C>T	XP_011541977.1:p.Gln1481Ter
XM_011543676.1:c.4441C>T	XP_011541978.1:p.Gln1481Ter
XM_011543677.1:c.1744C>T	XP_011541979.1:p.Gln582Ter
XM_011543678.1:c.4441C>T	XP_011541980.1:p.Gln1481Ter
XM_011543679.1:c.4441C>T	XP_011541981.1:p.Gln1481Ter
XM_017009963.2:c.4441C>T	XP_016865452.1:p.Gln1481Ter
XM_017009964.2:c.4441C>T	XP_016865453.1:p.Gln1481Ter
XM_017009965.1:c.4438C>T	XP_016865454.1:p.Gln1480Ter
XM_017009966.2:c.4441C>T	XP_016865455.1:p.Gln1481Ter
XM_017009967.1:c.4345C>T	XP_016865456.1:p.Gln1449Ter
XM_017009968.2:c.4441C>T	XP_016865457.1:p.Gln1481Ter
XM_017009969.2:c.4441C>T	XP_016865458.1:p.Gln1481Ter
XM_017009970.2:c.4441C>T	XP_016865459.1:p.Gln1481Ter
XM_017009971.2:c.4441C>T	XP_016865460.1:p.Gln1481Ter
XM_017009974.2:c.4441C>T	XP_016865463.1:p.Gln1481Ter