Canonical Allele Identifier: CA360392296

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90706356G>A , CM000667.2:g.90706356G>A	GRCh38
NC_000005.9:g.90002173G>A , CM000667.1:g.90002173G>A	GRCh37
NC_000005.8:g.90037929G>A	NCBI36
NG_007083.1:g.152557G>A
NG_007083.2:g.182013G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8692G>A MANE Select	NP_115495.3:p.Gly2898Arg
ENST00000405460.9:c.8692G>A MANE Select	ENSP00000384582.2:p.Gly2898Arg
NM_032119.3:c.8692G>A	NP_115495.3:p.Gly2898Arg
NR_003149.1:n.8705G>A
NR_003149.2:n.8708G>A
ENST00000405460.6:c.8692G>A	ENSP00000384582.2:p.Gly2898Arg
ENST00000509621.1:c.1389G>A
ENST00000639431.1:c.265+30147G>A	ENSP00000491057.1:n.265+30147G>A
ENST00000639473.1:n.4151G>A
ENST00000640012.1:c.2499G>A
ENST00000640374.1:n.1836G>A
ENST00000640403.1:c.5983G>A	ENSP00000492531.1:p.Gly1995Arg
ENST00000640779.1:c.3421G>A
XM_011543675.1:c.8689G>A	XP_011541977.1:p.Gly2897Arg
XM_011543676.1:c.8611G>A	XP_011541978.1:p.Gly2871Arg
XM_011543677.1:c.5995G>A	XP_011541979.1:p.Gly1999Arg
XM_011543678.1:c.8692G>A	XP_011541980.1:p.Gly2898Arg
XM_011543679.1:c.8692G>A	XP_011541981.1:p.Gly2898Arg
XM_017009963.2:c.8713G>A	XP_016865452.1:p.Gly2905Arg
XM_017009964.2:c.8710G>A	XP_016865453.1:p.Gly2904Arg
XM_017009965.1:c.8710G>A	XP_016865454.1:p.Gly2904Arg
XM_017009966.2:c.8632G>A	XP_016865455.1:p.Gly2878Arg
XM_017009967.1:c.8617G>A	XP_016865456.1:p.Gly2873Arg
XM_017009968.2:c.8713G>A	XP_016865457.1:p.Gly2905Arg
XM_017009969.2:c.8713G>A	XP_016865458.1:p.Gly2905Arg
XM_017009970.2:c.8713G>A	XP_016865459.1:p.Gly2905Arg
XM_017009971.2:c.8713G>A	XP_016865460.1:p.Gly2905Arg
XM_017009972.1:c.1831G>A	XP_016865461.1:p.Gly611Arg
XM_017009973.1:c.1810G>A	XP_016865462.1:p.Gly604Arg
XM_017009974.2:c.8713G>A	XP_016865463.1:p.Gly2905Arg