Canonical Allele Identifier: CA1826365419
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144511871C= , CM000670.2:g.144511871C= GRCh38
NC_000008.10:g.145737254C= , CM000670.1:g.145737254C= GRCh37
NC_000008.9:g.145708062C= NCBI36
NG_016430.1:g.10956G=
NG_016430.2:g.10956G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.3393+40G= MANE Select ENSP00000482313.2:n.3393+40G=
ENST00000301323.7:c.410+40G=
ENST00000529424.2:n.50-82G=
ENST00000531875.2:c.648+31G= ENSP00000477910.1:n.648+31G=
ENST00000617875.4:c.3393+40G= ENSP00000482313.1:n.3393+40G=
ENST00000621189.4:c.2322+40G= ENSP00000483145.1:n.2322+40G=
NM_004260.3:c.3393+40G= NP_004251.3:n.3393+40G=
XM_011517380.1:c.3468+40G= XP_011515682.1:n.3468+40G=
XM_011517381.1:c.3372+40G= XP_011515683.1:n.3372+40G=
XM_011517382.1:c.3276+40G= XP_011515684.1:n.3276+40G=
XM_011517383.1:c.3270+40G= XP_011515685.1:n.3270+40G=
XM_011517384.1:c.3195+40G= XP_011515686.1:n.3195+40G=
XM_011517385.1:c.2331+40G= XP_011515687.1:n.2331+40G=
XR_928366.1:n.3353-82G=
XR_928367.1:n.3448+40G=
XR_928368.1:n.3341+40G=
XM_011517384.3:c.3195+40G= XP_011515686.1:n.3195+40G=
XM_017013991.2:c.3598G= XP_016869480.1:p.Val1200=
XM_017013992.2:c.3523G= XP_016869481.1:p.Val1175=
XM_017013993.2:c.3508G= XP_016869482.1:p.Val1170=
XM_017013994.2:c.3502G= XP_016869483.1:p.Val1168=
XM_017013995.2:c.3433G= XP_016869484.1:p.Val1145=
XM_017013996.2:c.3558+40G= XP_016869485.1:n.3558+40G=
XM_017013997.2:c.3400G= XP_016869486.1:p.Val1134=
XM_017013998.1:c.3483+40G= XP_016869487.1:n.3483+40G=
XM_017013999.2:c.3310G= XP_016869488.1:p.Val1104=
XM_017014000.1:c.2461G= XP_016869489.1:p.Val821=
XM_017014001.2:c.2371G= XP_016869490.1:p.Val791=
XR_001745626.2:n.3439-82G=
XR_001745627.2:n.3534+40G=
XR_001745628.2:n.3425+40G=
XR_001745629.2:n.3288+40G=
XR_001745630.2:n.3090+40G=
NM_004260.4:c.3393+40G= MANE Select NP_004251.4:n.3393+40G=