Canonical Allele Identifier: CA275228
Gene: ADGRV1 HGNC NCBI

Linked Data

ClinVar Variation Id: 196961
ClinVar RCV Id: RCV000177853
dbSNP Id: rs794727584

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90703713del , CM000667.2:g.90703713del GRCh38
NC_000005.9:g.89999530del , CM000667.1:g.89999530del GRCh37
NC_000005.8:g.90035286del NCBI36
NG_007083.1:g.149914del
NG_007083.2:g.179370del

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.8204del MANE Select ENSP00000384582.2:p.Asn2735MetfsTer13
ENST00000639431.1:c.265+27504del ENSP00000491057.1:n.265+27504del
ENST00000639473.1:n.3663del
ENST00000640012.1:c.2011del
ENST00000640374.1:n.1348del
ENST00000640403.1:c.5495del ENSP00000492531.1:p.Asn1832MetfsTer13
ENST00000640779.1:c.2933del
ENST00000405460.6:c.8204del ENSP00000384582.2:p.Asn2735MetfsTer13
ENST00000509621.1:c.901del
NM_032119.3:c.8204del NP_115495.3:p.Asn2735MetfsTer13
NR_003149.1:n.8217del
XM_011543675.1:c.8201del XP_011541977.1:p.Asn2734MetfsTer13
XM_011543676.1:c.8123del XP_011541978.1:p.Asn2708MetfsTer13
XM_011543677.1:c.5507del XP_011541979.1:p.Asn1836MetfsTer13
XM_011543678.1:c.8204del XP_011541980.1:p.Asn2735MetfsTer13
XM_011543679.1:c.8204del XP_011541981.1:p.Asn2735MetfsTer13
NM_032119.4:c.8204del MANE Select NP_115495.3:p.Asn2735MetfsTer13
XM_017009963.2:c.8204del XP_016865452.1:p.Asn2735MetfsTer13
XM_017009964.2:c.8201del XP_016865453.1:p.Asn2734MetfsTer13
XM_017009965.1:c.8201del XP_016865454.1:p.Asn2734MetfsTer13
XM_017009966.2:c.8123del XP_016865455.1:p.Asn2708MetfsTer13
XM_017009967.1:c.8108del XP_016865456.1:p.Asn2703MetfsTer13
XM_017009968.2:c.8204del XP_016865457.1:p.Asn2735MetfsTer13
XM_017009969.2:c.8204del XP_016865458.1:p.Asn2735MetfsTer13
XM_017009970.2:c.8204del XP_016865459.1:p.Asn2735MetfsTer13
XM_017009971.2:c.8204del XP_016865460.1:p.Asn2735MetfsTer13
XM_017009972.1:c.1322del XP_016865461.1:p.Asn441MetfsTer13
XM_017009973.1:c.1322del XP_016865462.1:p.Asn441MetfsTer13
XM_017009974.2:c.8204del XP_016865463.1:p.Asn2735MetfsTer13
NR_003149.2:n.8220del