Canonical Allele Identifier: CA3342493

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965427G>A , CM000667.2:g.90965427G>A	GRCh38
NC_000005.9:g.90261244G>A , CM000667.1:g.90261244G>A	GRCh37
NC_000005.8:g.90297000G>A	NCBI36
NG_007083.1:g.411628G>A
NG_007083.2:g.441084G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17869G>A MANE Select	NP_115495.3:p.Ala5957Thr
ENST00000405460.9:c.17869G>A MANE Select	ENSP00000384582.2:p.Ala5957Thr
NM_032119.3:c.17869G>A	NP_115495.3:p.Ala5957Thr
NR_003149.1:n.17882G>A
NR_003149.2:n.17885G>A
ENST00000405460.6:c.17869G>A	ENSP00000384582.2:p.Ala5957Thr
ENST00000425867.2:c.4852G>A	ENSP00000392618.2:p.Ala1618Thr
ENST00000425867.3:c.6823G>A	ENSP00000392618.3:p.Ala2275Thr
ENST00000638510.1:n.5136G>A
ENST00000638990.1:c.1081G>A
ENST00000639431.1:c.266-19917G>A	ENSP00000491057.1:n.266-19917G>A
ENST00000639707.1:c.-48G>A	ENSP00000492328.1:n.-48G>A
ENST00000639821.1:c.-48G>A	ENSP00000492216.1:n.-48G>A
ENST00000640369.1:c.-48G>A	ENSP00000491401.1:n.-48G>A
ENST00000640407.1:c.4318G>A	ENSP00000491425.1:n.4318G>A
ENST00000640815.1:c.-48G>A	ENSP00000491767.1:n.-48G>A
XM_011543675.1:c.17866G>A	XP_011541977.1:p.Ala5956Thr
XM_011543676.1:c.17788G>A	XP_011541978.1:p.Ala5930Thr
XM_011543677.1:c.15172G>A	XP_011541979.1:p.Ala5058Thr
XM_017009963.2:c.17890G>A	XP_016865452.1:p.Ala5964Thr
XM_017009964.2:c.17887G>A	XP_016865453.1:p.Ala5963Thr
XM_017009965.1:c.17887G>A	XP_016865454.1:p.Ala5963Thr
XM_017009966.2:c.17809G>A	XP_016865455.1:p.Ala5937Thr
XM_017009967.1:c.17794G>A	XP_016865456.1:p.Ala5932Thr
XM_017009968.2:c.17710G>A	XP_016865457.1:p.Ala5904Thr
XM_017009969.2:c.17890G>A	XP_016865458.1:p.Ala5964Thr
XM_017009972.1:c.11008G>A	XP_016865461.1:p.Ala3670Thr
XM_017009973.1:c.10987G>A	XP_016865462.1:p.Ala3663Thr