Canonical Allele Identifier: CA1562859308
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692731_90692732delinsCG , CM000667.2:g.90692731_90692732delinsCG GRCh38
NC_000005.9:g.89988548_89988549delinsCG , CM000667.1:g.89988548_89988549delinsCG GRCh37
NC_000005.8:g.90024304_90024305delinsCG NCBI36
NG_007083.1:g.138932_138933delinsCG
NG_007083.2:g.168388_168389delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.7078_7079delinsCG MANE Select ENSP00000384582.2:p.Arg2360=
ENST00000639431.1:c.265+16522_265+16523delinsCG ENSP00000491057.1:n.265+16522_265+16523de...
ENST00000639473.1:n.2537_2538delinsCG
ENST00000640012.1:c.885_886delinsCG
ENST00000640374.1:n.222_223delinsCG
ENST00000640403.1:c.4369_4370delinsCG ENSP00000492531.1:p.Arg1457=
ENST00000640779.1:c.1807_1808delinsCG
ENST00000405460.6:c.7078_7079delinsCG ENSP00000384582.2:p.Arg2360=
NM_032119.3:c.7078_7079delinsCG NP_115495.3:p.Arg2360=
NR_003149.1:n.7091_7092delinsCG
XM_011543675.1:c.7075_7076delinsCG XP_011541977.1:p.Arg2359=
XM_011543676.1:c.6997_6998delinsCG XP_011541978.1:p.Arg2333=
XM_011543677.1:c.4381_4382delinsCG XP_011541979.1:p.Arg1461=
XM_011543678.1:c.7078_7079delinsCG XP_011541980.1:p.Arg2360=
XM_011543679.1:c.7078_7079delinsCG XP_011541981.1:p.Arg2360=
NM_032119.4:c.7078_7079delinsCG MANE Select NP_115495.3:p.Arg2360=
XM_017009963.2:c.7078_7079delinsCG XP_016865452.1:p.Arg2360=
XM_017009964.2:c.7075_7076delinsCG XP_016865453.1:p.Arg2359=
XM_017009965.1:c.7075_7076delinsCG XP_016865454.1:p.Arg2359=
XM_017009966.2:c.6997_6998delinsCG XP_016865455.1:p.Arg2333=
XM_017009967.1:c.6982_6983delinsCG XP_016865456.1:p.Arg2328=
XM_017009968.2:c.7078_7079delinsCG XP_016865457.1:p.Arg2360=
XM_017009969.2:c.7078_7079delinsCG XP_016865458.1:p.Arg2360=
XM_017009970.2:c.7078_7079delinsCG XP_016865459.1:p.Arg2360=
XM_017009971.2:c.7078_7079delinsCG XP_016865460.1:p.Arg2360=
XM_017009972.1:c.196_197delinsCG XP_016865461.1:p.Arg66=
XM_017009973.1:c.196_197delinsCG XP_016865462.1:p.Arg66=
XM_017009974.2:c.7078_7079delinsCG XP_016865463.1:p.Arg2360=
NR_003149.2:n.7094_7095delinsCG