Canonical Allele Identifier: CA360393698

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90708910G>A , CM000667.2:g.90708910G>A	GRCh38
NC_000005.9:g.90004727G>A , CM000667.1:g.90004727G>A	GRCh37
NC_000005.8:g.90040483G>A	NCBI36
NG_007083.1:g.155111G>A
NG_007083.2:g.184567G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8824+1G>A MANE Select	NP_115495.3:n.8824+1G>A
ENST00000405460.9:c.8824+1G>A MANE Select	ENSP00000384582.2:n.8824+1G>A
NM_032119.3:c.8824+1G>A	NP_115495.3:n.8824+1G>A
NR_003149.1:n.8837+1G>A
NR_003149.2:n.8840+1G>A
ENST00000405460.6:c.8824+1G>A	ENSP00000384582.2:n.8824+1G>A
ENST00000509621.1:c.1521+1G>A
ENST00000639431.1:c.265+32701G>A	ENSP00000491057.1:n.265+32701G>A
ENST00000639473.1:n.4283+1G>A
ENST00000640012.1:c.2631+1G>A
ENST00000640374.1:n.1968+1G>A
ENST00000640779.1:c.3553+1G>A
XM_011543675.1:c.8821+1G>A	XP_011541977.1:n.8821+1G>A
XM_011543676.1:c.8743+1G>A	XP_011541978.1:n.8743+1G>A
XM_011543677.1:c.6127+1G>A	XP_011541979.1:n.6127+1G>A
XM_011543678.1:c.8824+1G>A	XP_011541980.1:n.8824+1G>A
XM_011543679.1:c.8824+1G>A	XP_011541981.1:n.8824+1G>A
XM_017009963.2:c.8845+1G>A	XP_016865452.1:n.8845+1G>A
XM_017009964.2:c.8842+1G>A	XP_016865453.1:n.8842+1G>A
XM_017009965.1:c.8842+1G>A	XP_016865454.1:n.8842+1G>A
XM_017009966.2:c.8764+1G>A	XP_016865455.1:n.8764+1G>A
XM_017009967.1:c.8749+1G>A	XP_016865456.1:n.8749+1G>A
XM_017009968.2:c.8845+1G>A	XP_016865457.1:n.8845+1G>A
XM_017009969.2:c.8845+1G>A	XP_016865458.1:n.8845+1G>A
XM_017009970.2:c.8845+1G>A	XP_016865459.1:n.8845+1G>A
XM_017009971.2:c.8845+1G>A	XP_016865460.1:n.8845+1G>A
XM_017009972.1:c.1963+1G>A	XP_016865461.1:n.1963+1G>A
XM_017009973.1:c.1942+1G>A	XP_016865462.1:n.1942+1G>A
XM_017009974.2:c.8845+1G>A	XP_016865463.1:n.8845+1G>A