Canonical Allele Identifier: CA3341503

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90783232G>A , CM000667.2:g.90783232G>A	GRCh38
NC_000005.9:g.90079049G>A , CM000667.1:g.90079049G>A	GRCh37
NC_000005.8:g.90114805G>A	NCBI36
NG_007083.1:g.229433G>A
NG_007083.2:g.258889G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13340G>A MANE Select	NP_115495.3:p.Gly4447Asp
ENST00000405460.9:c.13340G>A MANE Select	ENSP00000384582.2:p.Gly4447Asp
NM_032119.3:c.13340G>A	NP_115495.3:p.Gly4447Asp
NR_003149.1:n.13353G>A
NR_003149.2:n.13356G>A
ENST00000405460.6:c.13340G>A	ENSP00000384582.2:p.Gly4447Asp
ENST00000425867.2:c.323G>A	ENSP00000392618.2:p.Gly108Asp
ENST00000425867.3:c.2294G>A	ENSP00000392618.3:p.Gly765Asp
ENST00000638510.1:n.607G>A
ENST00000639431.1:c.265+107023G>A	ENSP00000491057.1:n.265+107023G>A
XM_011543675.1:c.13337G>A	XP_011541977.1:p.Gly4446Asp
XM_011543676.1:c.13259G>A	XP_011541978.1:p.Gly4420Asp
XM_011543677.1:c.10643G>A	XP_011541979.1:p.Gly3548Asp
XM_011543678.1:c.13340G>A	XP_011541980.1:p.Gly4447Asp
XM_017009963.2:c.13361G>A	XP_016865452.1:p.Gly4454Asp
XM_017009964.2:c.13358G>A	XP_016865453.1:p.Gly4453Asp
XM_017009965.1:c.13358G>A	XP_016865454.1:p.Gly4453Asp
XM_017009966.2:c.13280G>A	XP_016865455.1:p.Gly4427Asp
XM_017009967.1:c.13265G>A	XP_016865456.1:p.Gly4422Asp
XM_017009968.2:c.13361G>A	XP_016865457.1:p.Gly4454Asp
XM_017009969.2:c.13361G>A	XP_016865458.1:p.Gly4454Asp
XM_017009970.2:c.13361G>A	XP_016865459.1:p.Gly4454Asp
XM_017009971.2:c.13361G>A	XP_016865460.1:p.Gly4454Asp
XM_017009972.1:c.6479G>A	XP_016865461.1:p.Gly2160Asp
XM_017009973.1:c.6458G>A	XP_016865462.1:p.Gly2153Asp