Canonical Allele Identifier: CA122811311

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791137C>T , CM000667.2:g.90791137C>T	GRCh38
NC_000005.9:g.90086954C>T , CM000667.1:g.90086954C>T	GRCh37
NC_000005.8:g.90122710C>T	NCBI36
NG_007083.1:g.237338C>T
NG_007083.2:g.266794C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14308C>T MANE Select	NP_115495.3:p.Arg4770Cys
ENST00000405460.9:c.14308C>T MANE Select	ENSP00000384582.2:p.Arg4770Cys
NM_032119.3:c.14308C>T	NP_115495.3:p.Arg4770Cys
NR_003149.1:n.14321C>T
NR_003149.2:n.14324C>T
ENST00000405460.6:c.14308C>T	ENSP00000384582.2:p.Arg4770Cys
ENST00000425867.2:c.1291C>T	ENSP00000392618.2:p.Arg431Cys
ENST00000425867.3:c.3262C>T	ENSP00000392618.3:p.Arg1088Cys
ENST00000638510.1:n.1575C>T
ENST00000638585.1:n.74C>T
ENST00000638975.1:c.937C>T	ENSP00000492630.1:p.Arg313Cys
ENST00000639431.1:c.265+114928C>T	ENSP00000491057.1:n.265+114928C>T
ENST00000640407.1:c.718C>T	ENSP00000491425.1:p.Arg240Cys
XM_011543675.1:c.14305C>T	XP_011541977.1:p.Arg4769Cys
XM_011543676.1:c.14227C>T	XP_011541978.1:p.Arg4743Cys
XM_011543677.1:c.11611C>T	XP_011541979.1:p.Arg3871Cys
XM_011543678.1:c.14308C>T	XP_011541980.1:p.Arg4770Cys
XM_017009963.2:c.14329C>T	XP_016865452.1:p.Arg4777Cys
XM_017009964.2:c.14326C>T	XP_016865453.1:p.Arg4776Cys
XM_017009965.1:c.14326C>T	XP_016865454.1:p.Arg4776Cys
XM_017009966.2:c.14248C>T	XP_016865455.1:p.Arg4750Cys
XM_017009967.1:c.14233C>T	XP_016865456.1:p.Arg4745Cys
XM_017009968.2:c.14329C>T	XP_016865457.1:p.Arg4777Cys
XM_017009969.2:c.14329C>T	XP_016865458.1:p.Arg4777Cys
XM_017009970.2:c.14329C>T	XP_016865459.1:p.Arg4777Cys
XM_017009971.2:c.14329C>T	XP_016865460.1:p.Arg4777Cys
XM_017009972.1:c.7447C>T	XP_016865461.1:p.Arg2483Cys
XM_017009973.1:c.7426C>T	XP_016865462.1:p.Arg2476Cys