Canonical Allele Identifier: CA360426970

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965518G>A , CM000667.2:g.90965518G>A	GRCh38
NC_000005.9:g.90261335G>A , CM000667.1:g.90261335G>A	GRCh37
NC_000005.8:g.90297091G>A	NCBI36
NG_007083.1:g.411719G>A
NG_007083.2:g.441175G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17960G>A MANE Select	NP_115495.3:p.Trp5987Ter
ENST00000405460.9:c.17960G>A MANE Select	ENSP00000384582.2:p.Trp5987Ter
NM_032119.3:c.17960G>A	NP_115495.3:p.Trp5987Ter
NR_003149.1:n.17973G>A
NR_003149.2:n.17976G>A
ENST00000405460.6:c.17960G>A	ENSP00000384582.2:p.Trp5987Ter
ENST00000425867.2:c.4943G>A	ENSP00000392618.2:p.Trp1648Ter
ENST00000425867.3:c.6914G>A	ENSP00000392618.3:p.Trp2305Ter
ENST00000638510.1:n.5227G>A
ENST00000638990.1:c.1172G>A
ENST00000639431.1:c.266-19826G>A	ENSP00000491057.1:n.266-19826G>A
ENST00000639707.1:c.44G>A	ENSP00000492328.1:p.Trp15Ter
ENST00000639821.1:c.44G>A	ENSP00000492216.1:p.Trp15Ter
ENST00000640369.1:c.44G>A	ENSP00000491401.1:p.Trp15Ter
ENST00000640407.1:c.4409G>A	ENSP00000491425.1:n.4409G>A
ENST00000640815.1:c.44G>A	ENSP00000491767.1:p.Trp15Ter
XM_011543675.1:c.17957G>A	XP_011541977.1:p.Trp5986Ter
XM_011543676.1:c.17879G>A	XP_011541978.1:p.Trp5960Ter
XM_011543677.1:c.15263G>A	XP_011541979.1:p.Trp5088Ter
XM_017009963.2:c.17981G>A	XP_016865452.1:p.Trp5994Ter
XM_017009964.2:c.17978G>A	XP_016865453.1:p.Trp5993Ter
XM_017009965.1:c.17978G>A	XP_016865454.1:p.Trp5993Ter
XM_017009966.2:c.17900G>A	XP_016865455.1:p.Trp5967Ter
XM_017009967.1:c.17885G>A	XP_016865456.1:p.Trp5962Ter
XM_017009968.2:c.17801G>A	XP_016865457.1:p.Trp5934Ter
XM_017009969.2:c.17981G>A	XP_016865458.1:p.Trp5994Ter
XM_017009972.1:c.11099G>A	XP_016865461.1:p.Trp3700Ter
XM_017009973.1:c.11078G>A	XP_016865462.1:p.Trp3693Ter