Canonical Allele Identifier: CA1562902182

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90790948G= , CM000667.2:g.90790948G=	GRCh38
NC_000005.9:g.90086765G= , CM000667.1:g.90086765G=	GRCh37
NC_000005.8:g.90122521G=	NCBI36
NG_007083.1:g.237149G=
NG_007083.2:g.266605G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14119G= MANE Select	NP_115495.3:p.Asp4707=
ENST00000405460.9:c.14119G= MANE Select	ENSP00000384582.2:p.Asp4707=
NM_032119.3:c.14119G=	NP_115495.3:p.Asp4707=
NR_003149.1:n.14132G=
NR_003149.2:n.14135G=
ENST00000405460.6:c.14119G=	ENSP00000384582.2:p.Asp4707=
ENST00000425867.2:c.1102G=	ENSP00000392618.2:p.Asp368=
ENST00000425867.3:c.3073G=	ENSP00000392618.3:p.Asp1025=
ENST00000638510.1:n.1386G=
ENST00000638975.1:c.748G=	ENSP00000492630.1:p.Asp250=
ENST00000639431.1:c.265+114739G=	ENSP00000491057.1:n.265+114739G=
ENST00000640407.1:c.529G=	ENSP00000491425.1:p.Asp177=
XM_011543675.1:c.14116G=	XP_011541977.1:p.Asp4706=
XM_011543676.1:c.14038G=	XP_011541978.1:p.Asp4680=
XM_011543677.1:c.11422G=	XP_011541979.1:p.Asp3808=
XM_011543678.1:c.14119G=	XP_011541980.1:p.Asp4707=
XM_017009963.2:c.14140G=	XP_016865452.1:p.Asp4714=
XM_017009964.2:c.14137G=	XP_016865453.1:p.Asp4713=
XM_017009965.1:c.14137G=	XP_016865454.1:p.Asp4713=
XM_017009966.2:c.14059G=	XP_016865455.1:p.Asp4687=
XM_017009967.1:c.14044G=	XP_016865456.1:p.Asp4682=
XM_017009968.2:c.14140G=	XP_016865457.1:p.Asp4714=
XM_017009969.2:c.14140G=	XP_016865458.1:p.Asp4714=
XM_017009970.2:c.14140G=	XP_016865459.1:p.Asp4714=
XM_017009971.2:c.14140G=	XP_016865460.1:p.Asp4714=
XM_017009972.1:c.7258G=	XP_016865461.1:p.Asp2420=
XM_017009973.1:c.7237G=	XP_016865462.1:p.Asp2413=