Canonical Allele Identifier: CA445410030

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90774191G>A , CM000667.2:g.90774191G>A	GRCh38
NC_000005.9:g.90070008G>A , CM000667.1:g.90070008G>A	GRCh37
NC_000005.8:g.90105764G>A	NCBI36
NG_007083.1:g.220392G>A
NG_007083.2:g.249848G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12291G>A MANE Select	NP_115495.3:p.Glu4097=
ENST00000405460.9:c.12291G>A MANE Select	ENSP00000384582.2:p.Glu4097=
NM_032119.3:c.12291G>A	NP_115495.3:p.Glu4097=
NR_003149.1:n.12304G>A
NR_003149.2:n.12307G>A
ENST00000405460.6:c.12291G>A	ENSP00000384582.2:p.Glu4097=
ENST00000425867.3:c.1245G>A	ENSP00000392618.3:p.Glu415=
ENST00000639431.1:c.265+97982G>A	ENSP00000491057.1:n.265+97982G>A
ENST00000640464.1:n.2710G>A
ENST00000640729.1:n.868G>A
XM_011543675.1:c.12288G>A	XP_011541977.1:p.Glu4096=
XM_011543676.1:c.12210G>A	XP_011541978.1:p.Glu4070=
XM_011543677.1:c.9594G>A	XP_011541979.1:p.Glu3198=
XM_011543678.1:c.12291G>A	XP_011541980.1:p.Glu4097=
XM_017009963.2:c.12312G>A	XP_016865452.1:p.Glu4104=
XM_017009964.2:c.12309G>A	XP_016865453.1:p.Glu4103=
XM_017009965.1:c.12309G>A	XP_016865454.1:p.Glu4103=
XM_017009966.2:c.12231G>A	XP_016865455.1:p.Glu4077=
XM_017009967.1:c.12216G>A	XP_016865456.1:p.Glu4072=
XM_017009968.2:c.12312G>A	XP_016865457.1:p.Glu4104=
XM_017009969.2:c.12312G>A	XP_016865458.1:p.Glu4104=
XM_017009970.2:c.12312G>A	XP_016865459.1:p.Glu4104=
XM_017009971.2:c.12312G>A	XP_016865460.1:p.Glu4104=
XM_017009972.1:c.5430G>A	XP_016865461.1:p.Glu1810=
XM_017009973.1:c.5409G>A	XP_016865462.1:p.Glu1803=