Canonical Allele Identifier: CA1562902244

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791103T= , CM000667.2:g.90791103T=	GRCh38
NC_000005.9:g.90086920T= , CM000667.1:g.90086920T=	GRCh37
NC_000005.8:g.90122676T=	NCBI36
NG_007083.1:g.237304T=
NG_007083.2:g.266760T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14274T= MANE Select	ENSP00000384582.2:p.Asp4758=
ENST00000425867.3:c.3228T=	ENSP00000392618.3:p.Asp1076=
ENST00000638510.1:n.1541T=
ENST00000638585.1:n.40T=
ENST00000638975.1:c.903T=	ENSP00000492630.1:p.Asp301=
ENST00000639431.1:c.265+114894T=	ENSP00000491057.1:n.265+114894T=
ENST00000640407.1:c.684T=	ENSP00000491425.1:p.Asp228=
ENST00000405460.6:c.14274T=	ENSP00000384582.2:p.Asp4758=
ENST00000425867.2:c.1257T=	ENSP00000392618.2:p.Asp419=
NM_032119.3:c.14274T=	NP_115495.3:p.Asp4758=
NR_003149.1:n.14287T=
XM_011543675.1:c.14271T=	XP_011541977.1:p.Asp4757=
XM_011543676.1:c.14193T=	XP_011541978.1:p.Asp4731=
XM_011543677.1:c.11577T=	XP_011541979.1:p.Asp3859=
XM_011543678.1:c.14274T=	XP_011541980.1:p.Asp4758=
NM_032119.4:c.14274T= MANE Select	NP_115495.3:p.Asp4758=
XM_017009963.2:c.14295T=	XP_016865452.1:p.Asp4765=
XM_017009964.2:c.14292T=	XP_016865453.1:p.Asp4764=
XM_017009965.1:c.14292T=	XP_016865454.1:p.Asp4764=
XM_017009966.2:c.14214T=	XP_016865455.1:p.Asp4738=
XM_017009967.1:c.14199T=	XP_016865456.1:p.Asp4733=
XM_017009968.2:c.14295T=	XP_016865457.1:p.Asp4765=
XM_017009969.2:c.14295T=	XP_016865458.1:p.Asp4765=
XM_017009970.2:c.14295T=	XP_016865459.1:p.Asp4765=
XM_017009971.2:c.14295T=	XP_016865460.1:p.Asp4765=
XM_017009972.1:c.7413T=	XP_016865461.1:p.Asp2471=
XM_017009973.1:c.7392T=	XP_016865462.1:p.Asp2464=
NR_003149.2:n.14290T=