Canonical Allele Identifier: CA1826365421
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144511874G= , CM000670.2:g.144511874G= GRCh38
NC_000008.10:g.145737257G= , CM000670.1:g.145737257G= GRCh37
NC_000008.9:g.145708065G= NCBI36
NG_016430.1:g.10953C=
NG_016430.2:g.10953C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.3393+37C= MANE Select ENSP00000482313.2:n.3393+37C=
ENST00000301323.7:c.410+37C=
ENST00000529424.2:n.50-85C=
ENST00000531875.2:c.648+28C= ENSP00000477910.1:n.648+28C=
ENST00000617875.4:c.3393+37C= ENSP00000482313.1:n.3393+37C=
ENST00000621189.4:c.2322+37C= ENSP00000483145.1:n.2322+37C=
NM_004260.3:c.3393+37C= NP_004251.3:n.3393+37C=
XM_011517380.1:c.3468+37C= XP_011515682.1:n.3468+37C=
XM_011517381.1:c.3372+37C= XP_011515683.1:n.3372+37C=
XM_011517382.1:c.3276+37C= XP_011515684.1:n.3276+37C=
XM_011517383.1:c.3270+37C= XP_011515685.1:n.3270+37C=
XM_011517384.1:c.3195+37C= XP_011515686.1:n.3195+37C=
XM_011517385.1:c.2331+37C= XP_011515687.1:n.2331+37C=
XR_928366.1:n.3353-85C=
XR_928367.1:n.3448+37C=
XR_928368.1:n.3341+37C=
XM_011517384.3:c.3195+37C= XP_011515686.1:n.3195+37C=
XM_017013991.2:c.3595C= XP_016869480.1:p.Gln1199=
XM_017013992.2:c.3520C= XP_016869481.1:p.Gln1174=
XM_017013993.2:c.3505C= XP_016869482.1:p.Gln1169=
XM_017013994.2:c.3499C= XP_016869483.1:p.Gln1167=
XM_017013995.2:c.3430C= XP_016869484.1:p.Gln1144=
XM_017013996.2:c.3558+37C= XP_016869485.1:n.3558+37C=
XM_017013997.2:c.3397C= XP_016869486.1:p.Gln1133=
XM_017013998.1:c.3483+37C= XP_016869487.1:n.3483+37C=
XM_017013999.2:c.3307C= XP_016869488.1:p.Gln1103=
XM_017014000.1:c.2458C= XP_016869489.1:p.Gln820=
XM_017014001.2:c.2368C= XP_016869490.1:p.Gln790=
XR_001745626.2:n.3439-85C=
XR_001745627.2:n.3534+37C=
XR_001745628.2:n.3425+37C=
XR_001745629.2:n.3288+37C=
XR_001745630.2:n.3090+37C=
NM_004260.4:c.3393+37C= MANE Select NP_004251.4:n.3393+37C=