Canonical Allele Identifier: CA2689129834
Gene: RECQL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2738267
ClinVar RCV Id: RCV003508917

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144517661_144517667dup , CM000670.2:g.144517661_144517667dup GRCh38
NC_000008.10:g.145743045_145743051dup , CM000670.1:g.145743045_145743051dup GRCh37
NC_000008.9:g.145713853_145713859dup NCBI36
NG_016430.1:g.5166_5172dup
NG_033083.1:g.4697_4703dup
NG_016430.2:g.5166_5172dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.85-26_85-20dup MANE Select ENSP00000482313.2:n.85-26_85-20dup
ENST00000617875.4:c.85-26_85-20dup ENSP00000482313.1:n.85-26_85-20dup
ENST00000621189.4:c.-1013_-1007dup ENSP00000483145.1:n.-1013_-1007dup
NM_004260.3:c.85-26_85-20dup NP_004251.3:n.85-26_85-20dup
XM_011517380.1:c.85-26_85-20dup XP_011515682.1:n.85-26_85-20dup
XM_011517381.1:c.85-26_85-20dup XP_011515683.1:n.85-26_85-20dup
XM_011517382.1:c.85-26_85-20dup XP_011515684.1:n.85-26_85-20dup
XM_011517383.1:c.85-26_85-20dup XP_011515685.1:n.85-26_85-20dup
XM_011517384.1:c.85-26_85-20dup XP_011515686.1:n.85-26_85-20dup
XR_928366.1:n.126-26_126-20dup
XR_928367.1:n.126-26_126-20dup
XR_928368.1:n.128-26_128-20dup
XM_011517384.3:c.85-26_85-20dup XP_011515686.1:n.85-26_85-20dup
XM_017013991.2:c.85-26_85-20dup XP_016869480.1:n.85-26_85-20dup
XM_017013992.2:c.85-26_85-20dup XP_016869481.1:n.85-26_85-20dup
XM_017013993.2:c.85-26_85-20dup XP_016869482.1:n.85-26_85-20dup
XM_017013994.2:c.85-26_85-20dup XP_016869483.1:n.85-26_85-20dup
XM_017013995.2:c.85-26_85-20dup XP_016869484.1:n.85-26_85-20dup
XM_017013996.2:c.85-26_85-20dup XP_016869485.1:n.85-26_85-20dup
XM_017013997.2:c.85-26_85-20dup XP_016869486.1:n.85-26_85-20dup
XM_017013998.1:c.85-26_85-20dup XP_016869487.1:n.85-26_85-20dup
XM_017013999.2:c.85-26_85-20dup XP_016869488.1:n.85-26_85-20dup
XR_001745626.2:n.122-26_122-20dup
XR_001745627.2:n.122-26_122-20dup
XR_001745628.2:n.122-26_122-20dup
XR_001745629.2:n.122-26_122-20dup
XR_001745630.2:n.122-26_122-20dup
NM_004260.4:c.85-26_85-20dup MANE Select NP_004251.4:n.85-26_85-20dup