Canonical Allele Identifier: CA561259819
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs1475526220

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692634del , CM000667.2:g.90692634del GRCh38
NC_000005.9:g.89988451del , CM000667.1:g.89988451del GRCh37
NC_000005.8:g.90024207del NCBI36
NG_007083.1:g.138835del
NG_007083.2:g.168291del

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.6981del MANE Select ENSP00000384582.2:p.Gly2328ValfsTer7
ENST00000639431.1:c.265+16425del ENSP00000491057.1:n.265+16425del
ENST00000639473.1:n.2440del
ENST00000640012.1:c.788del
ENST00000640374.1:n.125del
ENST00000640403.1:c.4272del ENSP00000492531.1:p.Gly1425ValfsTer7
ENST00000640779.1:c.1710del
ENST00000405460.6:c.6981del ENSP00000384582.2:p.Gly2328ValfsTer7
NM_032119.3:c.6981del NP_115495.3:p.Gly2328ValfsTer7
NR_003149.1:n.6994del
XM_011543675.1:c.6978del XP_011541977.1:p.Gly2327ValfsTer7
XM_011543676.1:c.6900del XP_011541978.1:p.Gly2301ValfsTer7
XM_011543677.1:c.4284del XP_011541979.1:p.Gly1429ValfsTer7
XM_011543678.1:c.6981del XP_011541980.1:p.Gly2328ValfsTer7
XM_011543679.1:c.6981del XP_011541981.1:p.Gly2328ValfsTer7
NM_032119.4:c.6981del MANE Select NP_115495.3:p.Gly2328ValfsTer7
XM_017009963.2:c.6981del XP_016865452.1:p.Gly2328ValfsTer7
XM_017009964.2:c.6978del XP_016865453.1:p.Gly2327ValfsTer7
XM_017009965.1:c.6978del XP_016865454.1:p.Gly2327ValfsTer7
XM_017009966.2:c.6900del XP_016865455.1:p.Gly2301ValfsTer7
XM_017009967.1:c.6885del XP_016865456.1:p.Gly2296ValfsTer7
XM_017009968.2:c.6981del XP_016865457.1:p.Gly2328ValfsTer7
XM_017009969.2:c.6981del XP_016865458.1:p.Gly2328ValfsTer7
XM_017009970.2:c.6981del XP_016865459.1:p.Gly2328ValfsTer7
XM_017009971.2:c.6981del XP_016865460.1:p.Gly2328ValfsTer7
XM_017009972.1:c.99del XP_016865461.1:p.Gly34ValfsTer7
XM_017009973.1:c.99del XP_016865462.1:p.Gly34ValfsTer7
XM_017009974.2:c.6981del XP_016865463.1:p.Gly2328ValfsTer7
NR_003149.2:n.6997del