Canonical Allele Identifier: CA261834
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90855808del , CM000667.2:g.90855808del GRCh38
NC_000005.9:g.90151625del , CM000667.1:g.90151625del GRCh37
NC_000005.8:g.90187381del NCBI36
NG_007083.1:g.302009del
NG_007083.2:g.331465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.17662del MANE Select ENSP00000384582.2:p.Ser5888HisfsTer?
ENST00000425867.3:c.6616del ENSP00000392618.3:p.Ser2206HisfsTer?
ENST00000638510.1:n.4929del
ENST00000638990.1:c.874del
ENST00000639431.1:c.266-129536del ENSP00000491057.1:n.266-129536del
ENST00000640407.1:c.4111del ENSP00000491425.1:n.4111del
ENST00000405460.6:c.17662del ENSP00000384582.2:p.Ser5888HisfsTer?
ENST00000425867.2:c.4645del ENSP00000392618.2:p.Ser1549HisfsTer?
ENST00000503852.1:n.210del
NM_032119.3:c.17662del NP_115495.3:p.Ser5888HisfsTer?
NR_003149.1:n.17675del
XM_011543675.1:c.17659del XP_011541977.1:p.Ser5887HisfsTer?
XM_011543676.1:c.17581del XP_011541978.1:p.Ser5861HisfsTer?
XM_011543677.1:c.14965del XP_011541979.1:p.Ser4989HisfsTer?
NM_032119.4:c.17662del MANE Select NP_115495.3:p.Ser5888HisfsTer?
XM_017009963.2:c.17683del XP_016865452.1:p.Ser5895HisfsTer?
XM_017009964.2:c.17680del XP_016865453.1:p.Ser5894HisfsTer?
XM_017009965.1:c.17680del XP_016865454.1:p.Ser5894HisfsTer?
XM_017009966.2:c.17602del XP_016865455.1:p.Ser5868HisfsTer?
XM_017009967.1:c.17587del XP_016865456.1:p.Ser5863HisfsTer?
XM_017009968.2:c.17503del XP_016865457.1:p.Ser5835HisfsTer?
XM_017009969.2:c.17683del XP_016865458.1:p.Ser5895HisfsTer?
XM_017009972.1:c.10801del XP_016865461.1:p.Ser3601HisfsTer?
XM_017009973.1:c.10780del XP_016865462.1:p.Ser3594HisfsTer?
NR_003149.2:n.17678del