Canonical Allele Identifier: CA1826365393
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144511828G= , CM000670.2:g.144511828G= GRCh38
NC_000008.10:g.145737211G= , CM000670.1:g.145737211G= GRCh37
NC_000008.9:g.145708019G= NCBI36
NG_016430.1:g.10999C=
NG_016430.2:g.10999C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.3394-39C= MANE Select ENSP00000482313.2:n.3394-39C=
ENST00000301323.7:c.411-39C=
ENST00000529424.2:n.50-39C=
ENST00000531875.2:c.649-39C= ENSP00000477910.1:n.649-39C=
ENST00000617875.4:c.3394-39C= ENSP00000482313.1:n.3394-39C=
ENST00000621189.4:c.2323-39C= ENSP00000483145.1:n.2323-39C=
NM_004260.3:c.3394-39C= NP_004251.3:n.3394-39C=
XM_011517380.1:c.3469-39C= XP_011515682.1:n.3469-39C=
XM_011517381.1:c.3373-39C= XP_011515683.1:n.3373-39C=
XM_011517382.1:c.3277-39C= XP_011515684.1:n.3277-39C=
XM_011517383.1:c.3271-39C= XP_011515685.1:n.3271-39C=
XM_011517384.1:c.3196-39C= XP_011515686.1:n.3196-39C=
XM_011517385.1:c.2332-39C= XP_011515687.1:n.2332-39C=
XR_928366.1:n.3353-39C=
XR_928367.1:n.3449-39C=
XR_928368.1:n.3342-39C=
XM_011517384.3:c.3196-39C= XP_011515686.1:n.3196-39C=
XM_017013991.2:c.3641C= XP_016869480.1:p.Thr1214=
XM_017013992.2:c.3566C= XP_016869481.1:p.Thr1189=
XM_017013993.2:c.3551C= XP_016869482.1:p.Thr1184=
XM_017013994.2:c.3545C= XP_016869483.1:p.Thr1182=
XM_017013995.2:c.3476C= XP_016869484.1:p.Thr1159=
XM_017013996.2:c.3559-39C= XP_016869485.1:n.3559-39C=
XM_017013997.2:c.3443C= XP_016869486.1:p.Thr1148=
XM_017013998.1:c.3484-39C= XP_016869487.1:n.3484-39C=
XM_017013999.2:c.3353C= XP_016869488.1:p.Thr1118=
XM_017014000.1:c.2504C= XP_016869489.1:p.Thr835=
XM_017014001.2:c.2414C= XP_016869490.1:p.Thr805=
XR_001745626.2:n.3439-39C=
XR_001745627.2:n.3535-39C=
XR_001745628.2:n.3426-39C=
XR_001745629.2:n.3289-39C=
XR_001745630.2:n.3091-39C=
NM_004260.4:c.3394-39C= MANE Select NP_004251.4:n.3394-39C=