Canonical Allele Identifier: CA2782589791
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144515854_144515855insCACACCCAAC , CM000670.2:g.144515854_144515855insCACACCCAAC GRCh38
NC_000008.10:g.145741238_145741239insCACACCCAAC , CM000670.1:g.145741238_145741239insCACACCCAAC GRCh37
NC_000008.9:g.145712046_145712047insCACACCCAAC NCBI36
NG_016430.1:g.6972_6973insGTTGGGTGTG
NG_033083.1:g.2890_2891insCACACCCAAC
NG_016430.2:g.6972_6973insGTTGGGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.1167_1168insGTTGGGTGTG MANE Select ENSP00000482313.2:p.Phe390ValfsTer?
ENST00000532846.2:c.52_53insGTTGGGTGTG
ENST00000617875.4:c.1167_1168insGTTGGGTGTG ENSP00000482313.1:p.Phe390ValfsTer?
ENST00000621189.4:c.96_97insGTTGGGTGTG ENSP00000483145.1:p.Phe33ValfsTer?
NM_004260.3:c.1167_1168insGTTGGGTGTG NP_004251.3:p.Phe390ValfsTer?
XM_011517380.1:c.1167_1168insGTTGGGTGTG XP_011515682.1:p.Phe390ValfsTer?
XM_011517381.1:c.1071_1072insGTTGGGTGTG XP_011515683.1:p.Phe358ValfsTer?
XM_011517382.1:c.1167_1168insGTTGGGTGTG XP_011515684.1:p.Phe390ValfsTer?
XM_011517383.1:c.1167_1168insGTTGGGTGTG XP_011515685.1:p.Phe390ValfsTer?
XM_011517384.1:c.1167_1168insGTTGGGTGTG XP_011515686.1:p.Phe390ValfsTer?
XM_011517385.1:c.34_35insGTTGGGTGTG XP_011515687.1:p.Phe12CysfsTer20
XR_928366.1:n.1208_1209insGTTGGGTGTG
XR_928367.1:n.1208_1209insGTTGGGTGTG
XR_928368.1:n.1210_1211insGTTGGGTGTG
XM_011517384.3:c.1167_1168insGTTGGGTGTG XP_011515686.1:p.Phe390ValfsTer?
XM_017013991.2:c.1167_1168insGTTGGGTGTG XP_016869480.1:p.Phe390ValfsTer?
XM_017013992.2:c.1167_1168insGTTGGGTGTG XP_016869481.1:p.Phe390ValfsTer?
XM_017013993.2:c.1167_1168insGTTGGGTGTG XP_016869482.1:p.Phe390ValfsTer?
XM_017013994.2:c.1071_1072insGTTGGGTGTG XP_016869483.1:p.Phe358ValfsTer?
XM_017013995.2:c.1167_1168insGTTGGGTGTG XP_016869484.1:p.Phe390ValfsTer?
XM_017013996.2:c.1167_1168insGTTGGGTGTG XP_016869485.1:p.Phe390ValfsTer?
XM_017013997.2:c.1167_1168insGTTGGGTGTG XP_016869486.1:p.Phe390ValfsTer?
XM_017013998.1:c.1167_1168insGTTGGGTGTG XP_016869487.1:p.Phe390ValfsTer?
XM_017013999.2:c.1167_1168insGTTGGGTGTG XP_016869488.1:p.Phe390ValfsTer?
XM_017014000.1:c.34_35insGTTGGGTGTG XP_016869489.1:p.Phe12CysfsTer20
XM_017014001.2:c.34_35insGTTGGGTGTG XP_016869490.1:p.Phe12CysfsTer20
XR_001745626.2:n.1204_1205insGTTGGGTGTG
XR_001745627.2:n.1204_1205insGTTGGGTGTG
XR_001745628.2:n.1204_1205insGTTGGGTGTG
XR_001745629.2:n.1204_1205insGTTGGGTGTG
XR_001745630.2:n.1204_1205insGTTGGGTGTG
NM_004260.4:c.1167_1168insGTTGGGTGTG MANE Select NP_004251.4:p.Phe390ValfsTer?