Canonical Allele Identifier: CA360429065

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985357G>A , CM000667.2:g.90985357G>A	GRCh38
NC_000005.9:g.90281174G>A , CM000667.1:g.90281174G>A	GRCh37
NC_000005.8:g.90316930G>A	NCBI36
NG_007083.1:g.431558G>A
NG_007083.2:g.461014G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17987G>A MANE Select	NP_115495.3:p.Trp5996Ter
ENST00000405460.9:c.17987G>A MANE Select	ENSP00000384582.2:p.Trp5996Ter
NM_032119.3:c.17987G>A	NP_115495.3:p.Trp5996Ter
NR_003149.1:n.18000G>A
NR_003149.2:n.18003G>A
ENST00000405460.6:c.17987G>A	ENSP00000384582.2:p.Trp5996Ter
ENST00000425867.2:c.4970G>A	ENSP00000392618.2:p.Trp1657Ter
ENST00000425867.3:c.6941G>A	ENSP00000392618.3:p.Trp2314Ter
ENST00000638510.1:n.5254G>A
ENST00000638990.1:c.1199G>A
ENST00000639431.1:c.279G>A	ENSP00000491057.1:p.Leu93=
ENST00000639707.1:c.71G>A	ENSP00000492328.1:p.Trp24Ter
ENST00000639821.1:c.71G>A	ENSP00000492216.1:p.Trp24Ter
ENST00000640369.1:c.71G>A	ENSP00000491401.1:p.Trp24Ter
ENST00000640407.1:c.4436G>A	ENSP00000491425.1:n.4436G>A
ENST00000640815.1:c.71G>A	ENSP00000491767.1:p.Trp24Ter
XM_011543675.1:c.17984G>A	XP_011541977.1:p.Trp5995Ter
XM_011543676.1:c.17906G>A	XP_011541978.1:p.Trp5969Ter
XM_011543677.1:c.15290G>A	XP_011541979.1:p.Trp5097Ter
XM_017009963.2:c.18008G>A	XP_016865452.1:p.Trp6003Ter
XM_017009964.2:c.18005G>A	XP_016865453.1:p.Trp6002Ter
XM_017009965.1:c.18005G>A	XP_016865454.1:p.Trp6002Ter
XM_017009966.2:c.17927G>A	XP_016865455.1:p.Trp5976Ter
XM_017009967.1:c.17912G>A	XP_016865456.1:p.Trp5971Ter
XM_017009968.2:c.17828G>A	XP_016865457.1:p.Trp5943Ter
XM_017009969.2:c.18008G>A	XP_016865458.1:p.Trp6003Ter
XM_017009972.1:c.11126G>A	XP_016865461.1:p.Trp3709Ter
XM_017009973.1:c.11105G>A	XP_016865462.1:p.Trp3702Ter