Canonical Allele Identifier: CA1562855109

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683966T= , CM000667.2:g.90683966T=	GRCh38
NC_000005.9:g.89979783T= , CM000667.1:g.89979783T=	GRCh37
NC_000005.8:g.90015539T=	NCBI36
NG_007083.1:g.130167T=
NG_007083.2:g.159623T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6045T= MANE Select	ENSP00000384582.2:p.Tyr2015=
ENST00000639431.1:c.265+7757T=	ENSP00000491057.1:n.265+7757T=
ENST00000639473.1:n.1504T=
ENST00000640012.1:c.165-1814T=
ENST00000640403.1:c.3336T=	ENSP00000492531.1:p.Tyr1112=
ENST00000640779.1:c.857T=
ENST00000405460.6:c.6045T=	ENSP00000384582.2:p.Tyr2015=
NM_032119.3:c.6045T=	NP_115495.3:p.Tyr2015=
NR_003149.1:n.6141T=
XM_011543675.1:c.6042T=	XP_011541977.1:p.Tyr2014=
XM_011543676.1:c.5964T=	XP_011541978.1:p.Tyr1988=
XM_011543677.1:c.3348T=	XP_011541979.1:p.Tyr1116=
XM_011543678.1:c.6045T=	XP_011541980.1:p.Tyr2015=
XM_011543679.1:c.6045T=	XP_011541981.1:p.Tyr2015=
NM_032119.4:c.6045T= MANE Select	NP_115495.3:p.Tyr2015=
XM_017009963.2:c.6045T=	XP_016865452.1:p.Tyr2015=
XM_017009964.2:c.6042T=	XP_016865453.1:p.Tyr2014=
XM_017009965.1:c.6042T=	XP_016865454.1:p.Tyr2014=
XM_017009966.2:c.5964T=	XP_016865455.1:p.Tyr1988=
XM_017009967.1:c.5949T=	XP_016865456.1:p.Tyr1983=
XM_017009968.2:c.6045T=	XP_016865457.1:p.Tyr2015=
XM_017009969.2:c.6045T=	XP_016865458.1:p.Tyr2015=
XM_017009970.2:c.6045T=	XP_016865459.1:p.Tyr2015=
XM_017009971.2:c.6045T=	XP_016865460.1:p.Tyr2015=
XM_017009973.1:c.-755T=	XP_016865462.1:n.-755T=
XM_017009974.2:c.6045T=	XP_016865463.1:p.Tyr2015=
NR_003149.2:n.6144T=