Canonical Allele Identifier: CA360389917

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90779031A>T , CM000667.2:g.90779031A>T	GRCh38
NC_000005.9:g.90074848A>T , CM000667.1:g.90074848A>T	GRCh37
NC_000005.8:g.90110604A>T	NCBI36
NG_007083.1:g.225232A>T
NG_007083.2:g.254688A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13016A>T MANE Select	NP_115495.3:p.Asp4339Val
ENST00000405460.9:c.13016A>T MANE Select	ENSP00000384582.2:p.Asp4339Val
NM_032119.3:c.13016A>T	NP_115495.3:p.Asp4339Val
NR_003149.1:n.13029A>T
NR_003149.2:n.13032A>T
ENST00000405460.6:c.13016A>T	ENSP00000384582.2:p.Asp4339Val
ENST00000425867.3:c.1970A>T	ENSP00000392618.3:p.Asp657Val
ENST00000639431.1:c.265+102822A>T	ENSP00000491057.1:n.265+102822A>T
ENST00000640464.1:n.3435A>T
XM_011543675.1:c.13013A>T	XP_011541977.1:p.Asp4338Val
XM_011543676.1:c.12935A>T	XP_011541978.1:p.Asp4312Val
XM_011543677.1:c.10319A>T	XP_011541979.1:p.Asp3440Val
XM_011543678.1:c.13016A>T	XP_011541980.1:p.Asp4339Val
XM_017009963.2:c.13037A>T	XP_016865452.1:p.Asp4346Val
XM_017009964.2:c.13034A>T	XP_016865453.1:p.Asp4345Val
XM_017009965.1:c.13034A>T	XP_016865454.1:p.Asp4345Val
XM_017009966.2:c.12956A>T	XP_016865455.1:p.Asp4319Val
XM_017009967.1:c.12941A>T	XP_016865456.1:p.Asp4314Val
XM_017009968.2:c.13037A>T	XP_016865457.1:p.Asp4346Val
XM_017009969.2:c.13037A>T	XP_016865458.1:p.Asp4346Val
XM_017009970.2:c.13037A>T	XP_016865459.1:p.Asp4346Val
XM_017009971.2:c.13037A>T	XP_016865460.1:p.Asp4346Val
XM_017009972.1:c.6155A>T	XP_016865461.1:p.Asp2052Val
XM_017009973.1:c.6134A>T	XP_016865462.1:p.Asp2045Val