Canonical Allele Identifier: CA2580078812
Gene: RECQL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2029920
ClinVar RCV Id: RCV002881062

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144515205del , CM000670.2:g.144515205del GRCh38
NC_000008.10:g.145740589del , CM000670.1:g.145740589del GRCh37
NC_000008.9:g.145711397del NCBI36
NG_016430.1:g.7625del
NG_033083.1:g.2241del
NG_016430.2:g.7625del

Transcript Alleles

HGVS Amino-acid Change
ENST00000688394.1:n.454del
ENST00000617875.6:c.1431del MANE Select ENSP00000482313.2:p.His478ThrfsTer?
ENST00000532846.2:c.316del
ENST00000617875.4:c.1431del ENSP00000482313.1:p.His478ThrfsTer?
ENST00000621189.4:c.360del ENSP00000483145.1:p.His121ThrfsTer?
NM_004260.3:c.1431del NP_004251.3:p.His478ThrfsTer?
XM_011517380.1:c.1431del XP_011515682.1:p.His478ThrfsTer?
XM_011517381.1:c.1335del XP_011515683.1:p.His446ThrfsTer?
XM_011517382.1:c.1431del XP_011515684.1:p.His478ThrfsTer?
XM_011517383.1:c.1431del XP_011515685.1:p.His478ThrfsTer?
XM_011517384.1:c.1431del XP_011515686.1:p.His478ThrfsTer?
XM_011517385.1:c.294del XP_011515687.1:p.His99ThrfsTer?
XR_928366.1:n.1472del
XR_928367.1:n.1472del
XR_928368.1:n.1474del
XM_011517384.3:c.1431del XP_011515686.1:p.His478ThrfsTer?
XM_017013991.2:c.1431del XP_016869480.1:p.His478ThrfsTer?
XM_017013992.2:c.1431del XP_016869481.1:p.His478ThrfsTer?
XM_017013993.2:c.1431del XP_016869482.1:p.His478ThrfsTer?
XM_017013994.2:c.1335del XP_016869483.1:p.His446ThrfsTer?
XM_017013995.2:c.1431del XP_016869484.1:p.His478ThrfsTer?
XM_017013996.2:c.1431del XP_016869485.1:p.His478ThrfsTer?
XM_017013997.2:c.1431del XP_016869486.1:p.His478ThrfsTer?
XM_017013998.1:c.1431del XP_016869487.1:p.His478ThrfsTer?
XM_017013999.2:c.1431del XP_016869488.1:p.His478ThrfsTer?
XM_017014000.1:c.294del XP_016869489.1:p.His99ThrfsTer?
XM_017014001.2:c.294del XP_016869490.1:p.His99ThrfsTer?
XR_001745626.2:n.1468del
XR_001745627.2:n.1468del
XR_001745628.2:n.1468del
XR_001745629.2:n.1468del
XR_001745630.2:n.1468del
NM_004260.4:c.1431del MANE Select NP_004251.4:p.His478ThrfsTer?