Canonical Allele Identifier: CA1826368791
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144516016_144516017delinsGC , CM000670.2:g.144516016_144516017delinsGC GRCh38
NC_000008.10:g.145741400_145741401delinsGC , CM000670.1:g.145741400_145741401delinsGC GRCh37
NC_000008.9:g.145712208_145712209delinsGC NCBI36
NG_016430.1:g.6810_6811delinsGC
NG_033083.1:g.3052_3053delinsGC
NG_016430.2:g.6810_6811delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.1102_1103delinsGC MANE Select ENSP00000482313.2:p.Ala368=
ENST00000524998.1:c.624_625delinsGC
ENST00000617875.4:c.1102_1103delinsGC ENSP00000482313.1:p.Ala368=
ENST00000621189.4:c.31_32delinsGC ENSP00000483145.1:p.Ala11=
NM_004260.3:c.1102_1103delinsGC NP_004251.3:p.Ala368=
XM_011517380.1:c.1102_1103delinsGC XP_011515682.1:p.Ala368=
XM_011517381.1:c.1006_1007delinsGC XP_011515683.1:p.Ala336=
XM_011517382.1:c.1102_1103delinsGC XP_011515684.1:p.Ala368=
XM_011517383.1:c.1102_1103delinsGC XP_011515685.1:p.Ala368=
XM_011517384.1:c.1102_1103delinsGC XP_011515686.1:p.Ala368=
XM_011517385.1:c.-32_-31delinsGC XP_011515687.1:n.-32_-31delinsGC
XR_928366.1:n.1143_1144delinsGC
XR_928367.1:n.1143_1144delinsGC
XR_928368.1:n.1145_1146delinsGC
XM_011517384.3:c.1102_1103delinsGC XP_011515686.1:p.Ala368=
XM_017013991.2:c.1102_1103delinsGC XP_016869480.1:p.Ala368=
XM_017013992.2:c.1102_1103delinsGC XP_016869481.1:p.Ala368=
XM_017013993.2:c.1102_1103delinsGC XP_016869482.1:p.Ala368=
XM_017013994.2:c.1006_1007delinsGC XP_016869483.1:p.Ala336=
XM_017013995.2:c.1102_1103delinsGC XP_016869484.1:p.Ala368=
XM_017013996.2:c.1102_1103delinsGC XP_016869485.1:p.Ala368=
XM_017013997.2:c.1102_1103delinsGC XP_016869486.1:p.Ala368=
XM_017013998.1:c.1102_1103delinsGC XP_016869487.1:p.Ala368=
XM_017013999.2:c.1102_1103delinsGC XP_016869488.1:p.Ala368=
XM_017014000.1:c.-32_-31delinsGC XP_016869489.1:n.-32_-31delinsGC
XM_017014001.2:c.-32_-31delinsGC XP_016869490.1:n.-32_-31delinsGC
XR_001745626.2:n.1139_1140delinsGC
XR_001745627.2:n.1139_1140delinsGC
XR_001745628.2:n.1139_1140delinsGC
XR_001745629.2:n.1139_1140delinsGC
XR_001745630.2:n.1139_1140delinsGC
NM_004260.4:c.1102_1103delinsGC MANE Select NP_004251.4:p.Ala368=