Canonical Allele Identifier: CA3340081

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90694491G>A , CM000667.2:g.90694491G>A	GRCh38
NC_000005.9:g.89990308G>A , CM000667.1:g.89990308G>A	GRCh37
NC_000005.8:g.90026064G>A	NCBI36
NG_007083.1:g.140692G>A
NG_007083.2:g.170148G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.7735G>A MANE Select	NP_115495.3:p.Val2579Met
ENST00000405460.9:c.7735G>A MANE Select	ENSP00000384582.2:p.Val2579Met
NM_032119.3:c.7735G>A	NP_115495.3:p.Val2579Met
NR_003149.1:n.7748G>A
NR_003149.2:n.7751G>A
ENST00000405460.6:c.7735G>A	ENSP00000384582.2:p.Val2579Met
ENST00000509621.1:c.432G>A
ENST00000639431.1:c.265+18282G>A	ENSP00000491057.1:n.265+18282G>A
ENST00000639473.1:n.3194G>A
ENST00000640012.1:c.1542G>A
ENST00000640374.1:n.879G>A
ENST00000640403.1:c.5026G>A	ENSP00000492531.1:p.Val1676Met
ENST00000640779.1:c.2464G>A
XM_011543675.1:c.7732G>A	XP_011541977.1:p.Val2578Met
XM_011543676.1:c.7654G>A	XP_011541978.1:p.Val2552Met
XM_011543677.1:c.5038G>A	XP_011541979.1:p.Val1680Met
XM_011543678.1:c.7735G>A	XP_011541980.1:p.Val2579Met
XM_011543679.1:c.7735G>A	XP_011541981.1:p.Val2579Met
XM_017009963.2:c.7735G>A	XP_016865452.1:p.Val2579Met
XM_017009964.2:c.7732G>A	XP_016865453.1:p.Val2578Met
XM_017009965.1:c.7732G>A	XP_016865454.1:p.Val2578Met
XM_017009966.2:c.7654G>A	XP_016865455.1:p.Val2552Met
XM_017009967.1:c.7639G>A	XP_016865456.1:p.Val2547Met
XM_017009968.2:c.7735G>A	XP_016865457.1:p.Val2579Met
XM_017009969.2:c.7735G>A	XP_016865458.1:p.Val2579Met
XM_017009970.2:c.7735G>A	XP_016865459.1:p.Val2579Met
XM_017009971.2:c.7735G>A	XP_016865460.1:p.Val2579Met
XM_017009972.1:c.853G>A	XP_016865461.1:p.Val285Met
XM_017009973.1:c.853G>A	XP_016865462.1:p.Val285Met
XM_017009974.2:c.7735G>A	XP_016865463.1:p.Val2579Met