Canonical Allele Identifier: CA1562882062
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs1754533331

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90745606dup , CM000667.2:g.90745606dup GRCh38
NC_000005.9:g.90041423dup , CM000667.1:g.90041423dup GRCh37
NC_000005.8:g.90077179dup NCBI36
NG_007083.1:g.191807dup
NG_007083.2:g.221263dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.10785dup MANE Select ENSP00000384582.2:p.Phe3596IlefsTer2
ENST00000639431.1:c.265+69397dup ENSP00000491057.1:n.265+69397dup
ENST00000640374.1:n.3929dup
ENST00000640464.1:n.1204dup
ENST00000405460.6:c.10785dup ENSP00000384582.2:p.Phe3596IlefsTer2
ENST00000509621.1:c.3482dup
NM_032119.3:c.10785dup NP_115495.3:p.Phe3596IlefsTer2
NR_003149.1:n.10798dup
XM_011543675.1:c.10782dup XP_011541977.1:p.Phe3595IlefsTer2
XM_011543676.1:c.10704dup XP_011541978.1:p.Phe3569IlefsTer2
XM_011543677.1:c.8088dup XP_011541979.1:p.Phe2697IlefsTer2
XM_011543678.1:c.10785dup XP_011541980.1:p.Phe3596IlefsTer2
XM_011543679.1:c.*7dup XP_011541981.1:n.*7dup
NM_032119.4:c.10785dup MANE Select NP_115495.3:p.Phe3596IlefsTer2
XM_017009963.2:c.10806dup XP_016865452.1:p.Phe3603IlefsTer2
XM_017009964.2:c.10803dup XP_016865453.1:p.Phe3602IlefsTer2
XM_017009965.1:c.10803dup XP_016865454.1:p.Phe3602IlefsTer2
XM_017009966.2:c.10725dup XP_016865455.1:p.Phe3576IlefsTer2
XM_017009967.1:c.10710dup XP_016865456.1:p.Phe3571IlefsTer2
XM_017009968.2:c.10806dup XP_016865457.1:p.Phe3603IlefsTer2
XM_017009969.2:c.10806dup XP_016865458.1:p.Phe3603IlefsTer2
XM_017009970.2:c.10806dup XP_016865459.1:p.Phe3603IlefsTer2
XM_017009971.2:c.10806dup XP_016865460.1:p.Phe3603IlefsTer2
XM_017009972.1:c.3924dup XP_016865461.1:p.Phe1309IlefsTer2
XM_017009973.1:c.3903dup XP_016865462.1:p.Phe1302IlefsTer2
XM_017009974.2:c.*7dup XP_016865463.1:n.*7dup
NR_003149.2:n.10801dup