Canonical Allele Identifier: CA3340409

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90711221G>A , CM000667.2:g.90711221G>A	GRCh38
NC_000005.9:g.90007038G>A , CM000667.1:g.90007038G>A	GRCh37
NC_000005.8:g.90042794G>A	NCBI36
NG_007083.1:g.157422G>A
NG_007083.2:g.186878G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8941G>A MANE Select	NP_115495.3:p.Val2981Ile
ENST00000405460.9:c.8941G>A MANE Select	ENSP00000384582.2:p.Val2981Ile
NM_032119.3:c.8941G>A	NP_115495.3:p.Val2981Ile
NR_003149.1:n.8954G>A
NR_003149.2:n.8957G>A
ENST00000405460.6:c.8941G>A	ENSP00000384582.2:p.Val2981Ile
ENST00000509621.1:c.1638G>A
ENST00000639431.1:c.265+35012G>A	ENSP00000491057.1:n.265+35012G>A
ENST00000639473.1:n.4400G>A
ENST00000640012.1:c.2748G>A
ENST00000640374.1:n.2085G>A
ENST00000640779.1:c.3670G>A
XM_011543675.1:c.8938G>A	XP_011541977.1:p.Val2980Ile
XM_011543676.1:c.8860G>A	XP_011541978.1:p.Val2954Ile
XM_011543677.1:c.6244G>A	XP_011541979.1:p.Val2082Ile
XM_011543678.1:c.8941G>A	XP_011541980.1:p.Val2981Ile
XM_011543679.1:c.8941G>A	XP_011541981.1:p.Val2981Ile
XM_017009963.2:c.8962G>A	XP_016865452.1:p.Val2988Ile
XM_017009964.2:c.8959G>A	XP_016865453.1:p.Val2987Ile
XM_017009965.1:c.8959G>A	XP_016865454.1:p.Val2987Ile
XM_017009966.2:c.8881G>A	XP_016865455.1:p.Val2961Ile
XM_017009967.1:c.8866G>A	XP_016865456.1:p.Val2956Ile
XM_017009968.2:c.8962G>A	XP_016865457.1:p.Val2988Ile
XM_017009969.2:c.8962G>A	XP_016865458.1:p.Val2988Ile
XM_017009970.2:c.8962G>A	XP_016865459.1:p.Val2988Ile
XM_017009971.2:c.8962G>A	XP_016865460.1:p.Val2988Ile
XM_017009972.1:c.2080G>A	XP_016865461.1:p.Val694Ile
XM_017009973.1:c.2059G>A	XP_016865462.1:p.Val687Ile
XM_017009974.2:c.8962G>A	XP_016865463.1:p.Val2988Ile