Canonical Allele Identifier: CA1826365560
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144512040G= , CM000670.2:g.144512040G= GRCh38
NC_000008.10:g.145737423G= , CM000670.1:g.145737423G= GRCh37
NC_000008.9:g.145708231G= NCBI36
NG_016430.1:g.10787C=
NG_016430.2:g.10787C=

Transcript Alleles

HGVS Amino-acid change
ENST00000617875.6:c.3264C= MANE Select ENSP00000482313.2:p.Cys1088=
ENST00000301323.7:c.281C=
ENST00000529424.2:n.50-251C=
ENST00000531875.2:c.510C= ENSP00000477910.1:p.Cys170=
ENST00000617875.4:c.3264C= ENSP00000482313.1:p.Cys1088=
ENST00000621189.4:c.2193C= ENSP00000483145.1:p.Cys731=
NM_004260.3:c.3264C= NP_004251.3:p.Cys1088=
XM_011517380.1:c.3339C= XP_011515682.1:p.Cys1113=
XM_011517381.1:c.3243C= XP_011515683.1:p.Cys1081=
XM_011517382.1:c.3147C= XP_011515684.1:p.Cys1049=
XM_011517383.1:c.3141C= XP_011515685.1:p.Cys1047=
XM_011517384.1:c.3066C= XP_011515686.1:p.Cys1022=
XM_011517385.1:c.2202C= XP_011515687.1:p.Cys734=
XR_928366.1:n.3352+104C=
XR_928367.1:n.3319C=
XR_928368.1:n.3212C=
XM_011517384.3:c.3066C= XP_011515686.1:p.Cys1022=
XM_017013991.2:c.3429C= XP_016869480.1:p.Cys1143=
XM_017013992.2:c.3354C= XP_016869481.1:p.Cys1118=
XM_017013993.2:c.3339C= XP_016869482.1:p.Cys1113=
XM_017013994.2:c.3333C= XP_016869483.1:p.Cys1111=
XM_017013995.2:c.3264C= XP_016869484.1:p.Cys1088=
XM_017013996.2:c.3429C= XP_016869485.1:p.Cys1143=
XM_017013997.2:c.3231C= XP_016869486.1:p.Cys1077=
XM_017013998.1:c.3354C= XP_016869487.1:p.Cys1118=
XM_017013999.2:c.3141C= XP_016869488.1:p.Cys1047=
XM_017014000.1:c.2292C= XP_016869489.1:p.Cys764=
XM_017014001.2:c.2202C= XP_016869490.1:p.Cys734=
XR_001745626.2:n.3438+104C=
XR_001745627.2:n.3405C=
XR_001745628.2:n.3296C=
XR_001745629.2:n.3159C=
XR_001745630.2:n.2961C=
NM_004260.4:c.3264C= MANE Select NP_004251.4:p.Cys1088=