Canonical Allele Identifier: CA560908602
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs1162769052

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90789763del , CM000667.2:g.90789763del GRCh38
NC_000005.9:g.90085580del , CM000667.1:g.90085580del GRCh37
NC_000005.8:g.90121336del NCBI36
NG_007083.1:g.235964del
NG_007083.2:g.265420del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.13955del MANE Select ENSP00000384582.2:p.Lys4652ArgfsTer?
ENST00000425867.3:c.2909del ENSP00000392618.3:p.Lys970ArgfsTer?
ENST00000638510.1:n.1222del
ENST00000638975.1:c.584del ENSP00000492630.1:p.Lys195ArgfsTer?
ENST00000639431.1:c.265+113554del ENSP00000491057.1:n.265+113554del
ENST00000640407.1:c.365del ENSP00000491425.1:p.Lys122ArgfsTer?
ENST00000405460.6:c.13955del ENSP00000384582.2:p.Lys4652ArgfsTer?
ENST00000425867.2:c.938del ENSP00000392618.2:p.Lys313ArgfsTer?
NM_032119.3:c.13955del NP_115495.3:p.Lys4652ArgfsTer?
NR_003149.1:n.13968del
XM_011543675.1:c.13952del XP_011541977.1:p.Lys4651ArgfsTer?
XM_011543676.1:c.13874del XP_011541978.1:p.Lys4625ArgfsTer?
XM_011543677.1:c.11258del XP_011541979.1:p.Lys3753ArgfsTer?
XM_011543678.1:c.13955del XP_011541980.1:p.Lys4652ArgfsTer?
NM_032119.4:c.13955del MANE Select NP_115495.3:p.Lys4652ArgfsTer?
XM_017009963.2:c.13976del XP_016865452.1:p.Lys4659ArgfsTer?
XM_017009964.2:c.13973del XP_016865453.1:p.Lys4658ArgfsTer?
XM_017009965.1:c.13973del XP_016865454.1:p.Lys4658ArgfsTer?
XM_017009966.2:c.13895del XP_016865455.1:p.Lys4632ArgfsTer?
XM_017009967.1:c.13880del XP_016865456.1:p.Lys4627ArgfsTer?
XM_017009968.2:c.13976del XP_016865457.1:p.Lys4659ArgfsTer?
XM_017009969.2:c.13976del XP_016865458.1:p.Lys4659ArgfsTer?
XM_017009970.2:c.13976del XP_016865459.1:p.Lys4659ArgfsTer?
XM_017009971.2:c.13976del XP_016865460.1:p.Lys4659ArgfsTer?
XM_017009972.1:c.7094del XP_016865461.1:p.Lys2365ArgfsTer?
XM_017009973.1:c.7073del XP_016865462.1:p.Lys2358ArgfsTer?
NR_003149.2:n.13971del