Canonical Allele Identifier: CA360411787

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811339G>A , CM000667.2:g.90811339G>A	GRCh38
NC_000005.9:g.90107156G>A , CM000667.1:g.90107156G>A	GRCh37
NC_000005.8:g.90142912G>A	NCBI36
NG_007083.1:g.257540G>A
NG_007083.2:g.286996G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16078+1G>A MANE Select	NP_115495.3:n.16078+1G>A
ENST00000405460.9:c.16078+1G>A MANE Select	ENSP00000384582.2:n.16078+1G>A
NM_032119.3:c.16078+1G>A	NP_115495.3:n.16078+1G>A
NR_003149.1:n.16091+1G>A
NR_003149.2:n.16094+1G>A
ENST00000405460.6:c.16078+1G>A	ENSP00000384582.2:n.16078+1G>A
ENST00000425867.2:c.3061+1G>A	ENSP00000392618.2:n.3061+1G>A
ENST00000425867.3:c.5032+1G>A	ENSP00000392618.3:n.5032+1G>A
ENST00000638510.1:n.3345+1G>A
ENST00000639431.1:c.265+135130G>A	ENSP00000491057.1:n.265+135130G>A
ENST00000640407.1:c.2488+1G>A	ENSP00000491425.1:n.2488+1G>A
XM_011543675.1:c.16075+1G>A	XP_011541977.1:n.16075+1G>A
XM_011543676.1:c.15997+1G>A	XP_011541978.1:n.15997+1G>A
XM_011543677.1:c.13381+1G>A	XP_011541979.1:n.13381+1G>A
XM_017009963.2:c.16099+1G>A	XP_016865452.1:n.16099+1G>A
XM_017009964.2:c.16096+1G>A	XP_016865453.1:n.16096+1G>A
XM_017009965.1:c.16096+1G>A	XP_016865454.1:n.16096+1G>A
XM_017009966.2:c.16018+1G>A	XP_016865455.1:n.16018+1G>A
XM_017009967.1:c.16003+1G>A	XP_016865456.1:n.16003+1G>A
XM_017009968.2:c.15919+1G>A	XP_016865457.1:n.15919+1G>A
XM_017009969.2:c.16099+1G>A	XP_016865458.1:n.16099+1G>A
XM_017009972.1:c.9217+1G>A	XP_016865461.1:n.9217+1G>A
XM_017009973.1:c.9196+1G>A	XP_016865462.1:n.9196+1G>A