Canonical Allele Identifier: CA176239

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90788182G>A , CM000667.2:g.90788182G>A	GRCh38
NC_000005.9:g.90083999G>A , CM000667.1:g.90083999G>A	GRCh37
NC_000005.8:g.90119755G>A	NCBI36
NG_007083.1:g.234383G>A
NG_007083.2:g.263839G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13765G>A MANE Select	NP_115495.3:p.Val4589Met
ENST00000405460.9:c.13765G>A MANE Select	ENSP00000384582.2:p.Val4589Met
NM_032119.3:c.13765G>A	NP_115495.3:p.Val4589Met
NR_003149.1:n.13778G>A
NR_003149.2:n.13781G>A
ENST00000405460.6:c.13765G>A	ENSP00000384582.2:p.Val4589Met
ENST00000425867.2:c.748G>A	ENSP00000392618.2:p.Val250Met
ENST00000425867.3:c.2719G>A	ENSP00000392618.3:p.Val907Met
ENST00000638510.1:n.1032G>A
ENST00000638975.1:c.394G>A	ENSP00000492630.1:p.Val132Met
ENST00000639431.1:c.265+111973G>A	ENSP00000491057.1:n.265+111973G>A
ENST00000640407.1:c.175G>A	ENSP00000491425.1:p.Val59Met
XM_011543675.1:c.13762G>A	XP_011541977.1:p.Val4588Met
XM_011543676.1:c.13684G>A	XP_011541978.1:p.Val4562Met
XM_011543677.1:c.11068G>A	XP_011541979.1:p.Val3690Met
XM_011543678.1:c.13765G>A	XP_011541980.1:p.Val4589Met
XM_017009963.2:c.13786G>A	XP_016865452.1:p.Val4596Met
XM_017009964.2:c.13783G>A	XP_016865453.1:p.Val4595Met
XM_017009965.1:c.13783G>A	XP_016865454.1:p.Val4595Met
XM_017009966.2:c.13705G>A	XP_016865455.1:p.Val4569Met
XM_017009967.1:c.13690G>A	XP_016865456.1:p.Val4564Met
XM_017009968.2:c.13786G>A	XP_016865457.1:p.Val4596Met
XM_017009969.2:c.13786G>A	XP_016865458.1:p.Val4596Met
XM_017009970.2:c.13786G>A	XP_016865459.1:p.Val4596Met
XM_017009971.2:c.13786G>A	XP_016865460.1:p.Val4596Met
XM_017009972.1:c.6904G>A	XP_016865461.1:p.Val2302Met
XM_017009973.1:c.6883G>A	XP_016865462.1:p.Val2295Met