Canonical Allele Identifier: CA1562902247

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791115A= , CM000667.2:g.90791115A=	GRCh38
NC_000005.9:g.90086932A= , CM000667.1:g.90086932A=	GRCh37
NC_000005.8:g.90122688A=	NCBI36
NG_007083.1:g.237316A=
NG_007083.2:g.266772A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14286A= MANE Select	ENSP00000384582.2:p.Gly4762=
ENST00000425867.3:c.3240A=	ENSP00000392618.3:p.Gly1080=
ENST00000638510.1:n.1553A=
ENST00000638585.1:n.52A=
ENST00000638975.1:c.915A=	ENSP00000492630.1:p.Gly305=
ENST00000639431.1:c.265+114906A=	ENSP00000491057.1:n.265+114906A=
ENST00000640407.1:c.696A=	ENSP00000491425.1:p.Gly232=
ENST00000405460.6:c.14286A=	ENSP00000384582.2:p.Gly4762=
ENST00000425867.2:c.1269A=	ENSP00000392618.2:p.Gly423=
NM_032119.3:c.14286A=	NP_115495.3:p.Gly4762=
NR_003149.1:n.14299A=
XM_011543675.1:c.14283A=	XP_011541977.1:p.Gly4761=
XM_011543676.1:c.14205A=	XP_011541978.1:p.Gly4735=
XM_011543677.1:c.11589A=	XP_011541979.1:p.Gly3863=
XM_011543678.1:c.14286A=	XP_011541980.1:p.Gly4762=
NM_032119.4:c.14286A= MANE Select	NP_115495.3:p.Gly4762=
XM_017009963.2:c.14307A=	XP_016865452.1:p.Gly4769=
XM_017009964.2:c.14304A=	XP_016865453.1:p.Gly4768=
XM_017009965.1:c.14304A=	XP_016865454.1:p.Gly4768=
XM_017009966.2:c.14226A=	XP_016865455.1:p.Gly4742=
XM_017009967.1:c.14211A=	XP_016865456.1:p.Gly4737=
XM_017009968.2:c.14307A=	XP_016865457.1:p.Gly4769=
XM_017009969.2:c.14307A=	XP_016865458.1:p.Gly4769=
XM_017009970.2:c.14307A=	XP_016865459.1:p.Gly4769=
XM_017009971.2:c.14307A=	XP_016865460.1:p.Gly4769=
XM_017009972.1:c.7425A=	XP_016865461.1:p.Gly2475=
XM_017009973.1:c.7404A=	XP_016865462.1:p.Gly2468=
NR_003149.2:n.14302A=