Canonical Allele Identifier: CA1562886236

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755173T= , CM000667.2:g.90755173T=	GRCh38
NC_000005.9:g.90050990T= , CM000667.1:g.90050990T=	GRCh37
NC_000005.8:g.90086746T=	NCBI36
NG_007083.1:g.201374T=
NG_007083.2:g.230830T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11568T= MANE Select	ENSP00000384582.2:p.Val3856=
ENST00000425867.3:c.699T=	ENSP00000392618.3:p.Val233=
ENST00000639431.1:c.265+78964T=	ENSP00000491057.1:n.265+78964T=
ENST00000640374.1:n.4712T=
ENST00000640464.1:n.1987T=
ENST00000405460.6:c.11568T=	ENSP00000384582.2:p.Val3856=
ENST00000509621.1:c.4265T=
NM_032119.3:c.11568T=	NP_115495.3:p.Val3856=
NR_003149.1:n.11581T=
XM_011543675.1:c.11565T=	XP_011541977.1:p.Val3855=
XM_011543676.1:c.11487T=	XP_011541978.1:p.Val3829=
XM_011543677.1:c.8871T=	XP_011541979.1:p.Val2957=
XM_011543678.1:c.11568T=	XP_011541980.1:p.Val3856=
NM_032119.4:c.11568T= MANE Select	NP_115495.3:p.Val3856=
XM_017009963.2:c.11589T=	XP_016865452.1:p.Val3863=
XM_017009964.2:c.11586T=	XP_016865453.1:p.Val3862=
XM_017009965.1:c.11586T=	XP_016865454.1:p.Val3862=
XM_017009966.2:c.11508T=	XP_016865455.1:p.Val3836=
XM_017009967.1:c.11493T=	XP_016865456.1:p.Val3831=
XM_017009968.2:c.11589T=	XP_016865457.1:p.Val3863=
XM_017009969.2:c.11589T=	XP_016865458.1:p.Val3863=
XM_017009970.2:c.11589T=	XP_016865459.1:p.Val3863=
XM_017009971.2:c.11589T=	XP_016865460.1:p.Val3863=
XM_017009972.1:c.4707T=	XP_016865461.1:p.Val1569=
XM_017009973.1:c.4686T=	XP_016865462.1:p.Val1562=
NR_003149.2:n.11584T=