Canonical Allele Identifier: CA1562870627

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716676G= , CM000667.2:g.90716676G=	GRCh38
NC_000005.9:g.90012493G= , CM000667.1:g.90012493G=	GRCh37
NC_000005.8:g.90048249G=	NCBI36
NG_007083.1:g.162877G=
NG_007083.2:g.192333G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9394G= MANE Select	ENSP00000384582.2:p.Asp3132=
ENST00000639431.1:c.265+40467G=	ENSP00000491057.1:n.265+40467G=
ENST00000639473.1:n.4853G=
ENST00000640012.1:c.3201G=
ENST00000640374.1:n.2538G=
ENST00000640779.1:c.4123G=
ENST00000405460.6:c.9394G=	ENSP00000384582.2:p.Asp3132=
ENST00000509621.1:c.2091G=
NM_032119.3:c.9394G=	NP_115495.3:p.Asp3132=
NR_003149.1:n.9407G=
XM_011543675.1:c.9391G=	XP_011541977.1:p.Asp3131=
XM_011543676.1:c.9313G=	XP_011541978.1:p.Asp3105=
XM_011543677.1:c.6697G=	XP_011541979.1:p.Asp2233=
XM_011543678.1:c.9394G=	XP_011541980.1:p.Asp3132=
XM_011543679.1:c.9394G=	XP_011541981.1:p.Asp3132=
XR_948560.1:n.272-867C=
NM_032119.4:c.9394G= MANE Select	NP_115495.3:p.Asp3132=
XM_017009963.2:c.9415G=	XP_016865452.1:p.Asp3139=
XM_017009964.2:c.9412G=	XP_016865453.1:p.Asp3138=
XM_017009965.1:c.9412G=	XP_016865454.1:p.Asp3138=
XM_017009966.2:c.9334G=	XP_016865455.1:p.Asp3112=
XM_017009967.1:c.9319G=	XP_016865456.1:p.Asp3107=
XM_017009968.2:c.9415G=	XP_016865457.1:p.Asp3139=
XM_017009969.2:c.9415G=	XP_016865458.1:p.Asp3139=
XM_017009970.2:c.9415G=	XP_016865459.1:p.Asp3139=
XM_017009971.2:c.9415G=	XP_016865460.1:p.Asp3139=
XM_017009972.1:c.2533G=	XP_016865461.1:p.Asp845=
XM_017009973.1:c.2512G=	XP_016865462.1:p.Asp838=
XM_017009974.2:c.9415G=	XP_016865463.1:p.Asp3139=
XR_001742802.1:n.2523-867C=
NR_003149.2:n.9410G=