Canonical Allele Identifier: CA1562859302
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692724_90692726delinsGGT , CM000667.2:g.90692724_90692726delinsGGT GRCh38
NC_000005.9:g.89988541_89988543delinsGGT , CM000667.1:g.89988541_89988543delinsGGT GRCh37
NC_000005.8:g.90024297_90024299delinsGGT NCBI36
NG_007083.1:g.138925_138927delinsGGT
NG_007083.2:g.168381_168383delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7071_7073delinsGGT MANE Select ENSP00000384582.2:p.Met2357=
ENST00000639431.1:c.265+16515_265+16517delinsGGT ENSP00000491057.1:n.265+16515_265+16517delinsGGT
ENST00000639473.1:n.2530_2532delinsGGT
ENST00000640012.1:c.878_880delinsGGT
ENST00000640374.1:n.215_217delinsGGT
ENST00000640403.1:c.4362_4364delinsGGT ENSP00000492531.1:p.Met1454=
ENST00000640779.1:c.1800_1802delinsGGT
ENST00000405460.6:c.7071_7073delinsGGT ENSP00000384582.2:p.Met2357=
NM_032119.3:c.7071_7073delinsGGT NP_115495.3:p.Met2357=
NR_003149.1:n.7084_7086delinsGGT
XM_011543675.1:c.7068_7070delinsGGT XP_011541977.1:p.Met2356=
XM_011543676.1:c.6990_6992delinsGGT XP_011541978.1:p.Met2330=
XM_011543677.1:c.4374_4376delinsGGT XP_011541979.1:p.Met1458=
XM_011543678.1:c.7071_7073delinsGGT XP_011541980.1:p.Met2357=
XM_011543679.1:c.7071_7073delinsGGT XP_011541981.1:p.Met2357=
NM_032119.4:c.7071_7073delinsGGT MANE Select NP_115495.3:p.Met2357=
XM_017009963.2:c.7071_7073delinsGGT XP_016865452.1:p.Met2357=
XM_017009964.2:c.7068_7070delinsGGT XP_016865453.1:p.Met2356=
XM_017009965.1:c.7068_7070delinsGGT XP_016865454.1:p.Met2356=
XM_017009966.2:c.6990_6992delinsGGT XP_016865455.1:p.Met2330=
XM_017009967.1:c.6975_6977delinsGGT XP_016865456.1:p.Met2325=
XM_017009968.2:c.7071_7073delinsGGT XP_016865457.1:p.Met2357=
XM_017009969.2:c.7071_7073delinsGGT XP_016865458.1:p.Met2357=
XM_017009970.2:c.7071_7073delinsGGT XP_016865459.1:p.Met2357=
XM_017009971.2:c.7071_7073delinsGGT XP_016865460.1:p.Met2357=
XM_017009972.1:c.189_191delinsGGT XP_016865461.1:p.Met63=
XM_017009973.1:c.189_191delinsGGT XP_016865462.1:p.Met63=
XM_017009974.2:c.7071_7073delinsGGT XP_016865463.1:p.Met2357=
NR_003149.2:n.7087_7089delinsGGT