Canonical Allele Identifier: CA1826370070
Gene: RECQL4 HGNC NCBI

Linked Data

dbSNP Id: rs1815418482

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144517678dup , CM000670.2:g.144517678dup GRCh38
NC_000008.10:g.145743062dup , CM000670.1:g.145743062dup GRCh37
NC_000008.9:g.145713870dup NCBI36
NG_016430.1:g.5152dup
NG_033083.1:g.4714dup
NG_016430.2:g.5152dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.84+26dup MANE Select ENSP00000482313.2:n.84+26dup
ENST00000617875.4:c.84+26dup ENSP00000482313.1:n.84+26dup
ENST00000621189.4:c.-1027dup ENSP00000483145.1:n.-1027dup
NM_004260.3:c.84+26dup NP_004251.3:n.84+26dup
XM_011517380.1:c.84+26dup XP_011515682.1:n.84+26dup
XM_011517381.1:c.84+26dup XP_011515683.1:n.84+26dup
XM_011517382.1:c.84+26dup XP_011515684.1:n.84+26dup
XM_011517383.1:c.84+26dup XP_011515685.1:n.84+26dup
XM_011517384.1:c.84+26dup XP_011515686.1:n.84+26dup
XR_928366.1:n.125+26dup
XR_928367.1:n.125+26dup
XR_928368.1:n.127+26dup
XM_011517384.3:c.84+26dup XP_011515686.1:n.84+26dup
XM_017013991.2:c.84+26dup XP_016869480.1:n.84+26dup
XM_017013992.2:c.84+26dup XP_016869481.1:n.84+26dup
XM_017013993.2:c.84+26dup XP_016869482.1:n.84+26dup
XM_017013994.2:c.84+26dup XP_016869483.1:n.84+26dup
XM_017013995.2:c.84+26dup XP_016869484.1:n.84+26dup
XM_017013996.2:c.84+26dup XP_016869485.1:n.84+26dup
XM_017013997.2:c.84+26dup XP_016869486.1:n.84+26dup
XM_017013998.1:c.84+26dup XP_016869487.1:n.84+26dup
XM_017013999.2:c.84+26dup XP_016869488.1:n.84+26dup
XR_001745626.2:n.121+26dup
XR_001745627.2:n.121+26dup
XR_001745628.2:n.121+26dup
XR_001745629.2:n.121+26dup
XR_001745630.2:n.121+26dup
NM_004260.4:c.84+26dup MANE Select NP_004251.4:n.84+26dup