Canonical Allele Identifier: CA1826368658

Gene: RECQL4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144515854_144515856delinsAAC , CM000670.2:g.144515854_144515856delinsAAC	GRCh38
NC_000008.10:g.145741238_145741240delinsAAC , CM000670.1:g.145741238_145741240delinsAAC	GRCh37
NC_000008.9:g.145712046_145712048delinsAAC	NCBI36
NG_016430.1:g.6971_6973delinsGTT
NG_033083.1:g.2890_2892delinsAAC
NG_016430.2:g.6971_6973delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617875.6:c.1166_1168delinsGTT MANE Select	ENSP00000482313.2:p.Cys389=
ENST00000532846.2:c.51_53delinsGTT
ENST00000617875.4:c.1166_1168delinsGTT	ENSP00000482313.1:p.Cys389=
ENST00000621189.4:c.95_97delinsGTT	ENSP00000483145.1:p.Cys32=
NM_004260.3:c.1166_1168delinsGTT	NP_004251.3:p.Cys389=
XM_011517380.1:c.1166_1168delinsGTT	XP_011515682.1:p.Cys389=
XM_011517381.1:c.1070_1072delinsGTT	XP_011515683.1:p.Cys357=
XM_011517382.1:c.1166_1168delinsGTT	XP_011515684.1:p.Cys389=
XM_011517383.1:c.1166_1168delinsGTT	XP_011515685.1:p.Cys389=
XM_011517384.1:c.1166_1168delinsGTT	XP_011515686.1:p.Cys389=
XM_011517385.1:c.33_35delinsGTT	XP_011515687.1:p.Val11=
XR_928366.1:n.1207_1209delinsGTT
XR_928367.1:n.1207_1209delinsGTT
XR_928368.1:n.1209_1211delinsGTT
XM_011517384.3:c.1166_1168delinsGTT	XP_011515686.1:p.Cys389=
XM_017013991.2:c.1166_1168delinsGTT	XP_016869480.1:p.Cys389=
XM_017013992.2:c.1166_1168delinsGTT	XP_016869481.1:p.Cys389=
XM_017013993.2:c.1166_1168delinsGTT	XP_016869482.1:p.Cys389=
XM_017013994.2:c.1070_1072delinsGTT	XP_016869483.1:p.Cys357=
XM_017013995.2:c.1166_1168delinsGTT	XP_016869484.1:p.Cys389=
XM_017013996.2:c.1166_1168delinsGTT	XP_016869485.1:p.Cys389=
XM_017013997.2:c.1166_1168delinsGTT	XP_016869486.1:p.Cys389=
XM_017013998.1:c.1166_1168delinsGTT	XP_016869487.1:p.Cys389=
XM_017013999.2:c.1166_1168delinsGTT	XP_016869488.1:p.Cys389=
XM_017014000.1:c.33_35delinsGTT	XP_016869489.1:p.Val11=
XM_017014001.2:c.33_35delinsGTT	XP_016869490.1:p.Val11=
XR_001745626.2:n.1203_1205delinsGTT
XR_001745627.2:n.1203_1205delinsGTT
XR_001745628.2:n.1203_1205delinsGTT
XR_001745629.2:n.1203_1205delinsGTT
XR_001745630.2:n.1203_1205delinsGTT
NM_004260.4:c.1166_1168delinsGTT MANE Select	NP_004251.4:p.Cys389=