Canonical Allele Identifier: CA1826365401
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144511838A= , CM000670.2:g.144511838A= GRCh38
NC_000008.10:g.145737221A= , CM000670.1:g.145737221A= GRCh37
NC_000008.9:g.145708029A= NCBI36
NG_016430.1:g.10989T=
NG_016430.2:g.10989T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.3394-49T= MANE Select ENSP00000482313.2:n.3394-49T=
ENST00000301323.7:c.411-49T=
ENST00000529424.2:n.50-49T=
ENST00000531875.2:c.649-49T= ENSP00000477910.1:n.649-49T=
ENST00000617875.4:c.3394-49T= ENSP00000482313.1:n.3394-49T=
ENST00000621189.4:c.2323-49T= ENSP00000483145.1:n.2323-49T=
NM_004260.3:c.3394-49T= NP_004251.3:n.3394-49T=
XM_011517380.1:c.3469-49T= XP_011515682.1:n.3469-49T=
XM_011517381.1:c.3373-49T= XP_011515683.1:n.3373-49T=
XM_011517382.1:c.3277-49T= XP_011515684.1:n.3277-49T=
XM_011517383.1:c.3271-49T= XP_011515685.1:n.3271-49T=
XM_011517384.1:c.3196-49T= XP_011515686.1:n.3196-49T=
XM_011517385.1:c.2332-49T= XP_011515687.1:n.2332-49T=
XR_928366.1:n.3353-49T=
XR_928367.1:n.3449-49T=
XR_928368.1:n.3342-49T=
XM_011517384.3:c.3196-49T= XP_011515686.1:n.3196-49T=
XM_017013991.2:c.3631T= XP_016869480.1:p.Cys1211=
XM_017013992.2:c.3556T= XP_016869481.1:p.Cys1186=
XM_017013993.2:c.3541T= XP_016869482.1:p.Cys1181=
XM_017013994.2:c.3535T= XP_016869483.1:p.Cys1179=
XM_017013995.2:c.3466T= XP_016869484.1:p.Cys1156=
XM_017013996.2:c.3559-49T= XP_016869485.1:n.3559-49T=
XM_017013997.2:c.3433T= XP_016869486.1:p.Cys1145=
XM_017013998.1:c.3484-49T= XP_016869487.1:n.3484-49T=
XM_017013999.2:c.3343T= XP_016869488.1:p.Cys1115=
XM_017014000.1:c.2494T= XP_016869489.1:p.Cys832=
XM_017014001.2:c.2404T= XP_016869490.1:p.Cys802=
XR_001745626.2:n.3439-49T=
XR_001745627.2:n.3535-49T=
XR_001745628.2:n.3426-49T=
XR_001745629.2:n.3289-49T=
XR_001745630.2:n.3091-49T=
NM_004260.4:c.3394-49T= MANE Select NP_004251.4:n.3394-49T=