Canonical Allele Identifier: CA253958
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90708875del , CM000667.2:g.90708875del GRCh38
NC_000005.9:g.90004692del , CM000667.1:g.90004692del GRCh37
NC_000005.8:g.90040448del NCBI36
NG_007083.1:g.155076del
NG_007083.2:g.184532del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.8790del MANE Select ENSP00000384582.2:p.Met2931TrpfsTer11
ENST00000639431.1:c.265+32666del ENSP00000491057.1:n.265+32666del
ENST00000639473.1:n.4249del
ENST00000640012.1:c.2597del
ENST00000640374.1:n.1934del
ENST00000640403.1:c.6081del ENSP00000492531.1:p.Met2028TrpfsTer11
ENST00000640779.1:c.3519del
ENST00000405460.6:c.8790del ENSP00000384582.2:p.Met2931TrpfsTer11
ENST00000509621.1:c.1487del
NM_032119.3:c.8790del NP_115495.3:p.Met2931TrpfsTer11
NR_003149.1:n.8803del
XM_011543675.1:c.8787del XP_011541977.1:p.Met2930TrpfsTer11
XM_011543676.1:c.8709del XP_011541978.1:p.Met2904TrpfsTer11
XM_011543677.1:c.6093del XP_011541979.1:p.Met2032TrpfsTer11
XM_011543678.1:c.8790del XP_011541980.1:p.Met2931TrpfsTer11
XM_011543679.1:c.8790del XP_011541981.1:p.Met2931TrpfsTer11
NM_032119.4:c.8790del MANE Select NP_115495.3:p.Met2931TrpfsTer11
XM_017009963.2:c.8811del XP_016865452.1:p.Met2938TrpfsTer11
XM_017009964.2:c.8808del XP_016865453.1:p.Met2937TrpfsTer11
XM_017009965.1:c.8808del XP_016865454.1:p.Met2937TrpfsTer11
XM_017009966.2:c.8730del XP_016865455.1:p.Met2911TrpfsTer11
XM_017009967.1:c.8715del XP_016865456.1:p.Met2906TrpfsTer11
XM_017009968.2:c.8811del XP_016865457.1:p.Met2938TrpfsTer11
XM_017009969.2:c.8811del XP_016865458.1:p.Met2938TrpfsTer11
XM_017009970.2:c.8811del XP_016865459.1:p.Met2938TrpfsTer11
XM_017009971.2:c.8811del XP_016865460.1:p.Met2938TrpfsTer11
XM_017009972.1:c.1929del XP_016865461.1:p.Met644TrpfsTer11
XM_017009973.1:c.1908del XP_016865462.1:p.Met637TrpfsTer11
XM_017009974.2:c.8811del XP_016865463.1:p.Met2938TrpfsTer11
NR_003149.2:n.8806del