Canonical Allele Identifier: CA1826369996

Gene: RECQL4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144517576_144517584delinsCCCCCGCCG , CM000670.2:g.144517576_144517584delinsCCCCCGCCG	GRCh38
NC_000008.10:g.145742960_145742968delinsCCCCCGCCG , CM000670.1:g.145742960_145742968delinsCCCCCGCCG	GRCh37
NC_000008.9:g.145713768_145713776delinsCCCCCGCCG	NCBI36
NG_016430.1:g.5243_5251delinsCGGCGGGGG
NG_033083.1:g.4612_4620delinsCCCCCGCCG
NG_016430.2:g.5243_5251delinsCGGCGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617875.6:c.118+18_118+26delinsCGGCGGGGG MANE Select	ENSP00000482313.2:n.118+18_118+26delinsCGGCGGGGG
ENST00000534538.1:c.27+18_28-23delinsCGGCGGGGG
ENST00000617875.4:c.118+18_118+26delinsCGGCGGGGG	ENSP00000482313.1:n.118+18_118+26delinsCGGCGGGGG
ENST00000621189.4:c.-954+18_-954+26delinsCGGCGGGGG	ENSP00000483145.1:n.-954+18_-954+26delinsCGGCGGGGG
NM_004260.3:c.118+18_118+26delinsCGGCGGGGG	NP_004251.3:n.118+18_118+26delinsCGGCGGGGG
XM_011517380.1:c.118+18_118+26delinsCGGCGGGGG	XP_011515682.1:n.118+18_118+26delinsCGGCGGGGG
XM_011517381.1:c.118+18_118+26delinsCGGCGGGGG	XP_011515683.1:n.118+18_118+26delinsCGGCGGGGG
XM_011517382.1:c.118+18_118+26delinsCGGCGGGGG	XP_011515684.1:n.118+18_118+26delinsCGGCGGGGG
XM_011517383.1:c.118+18_118+26delinsCGGCGGGGG	XP_011515685.1:n.118+18_118+26delinsCGGCGGGGG
XM_011517384.1:c.118+18_118+26delinsCGGCGGGGG	XP_011515686.1:n.118+18_118+26delinsCGGCGGGGG
XR_928366.1:n.159+18_159+26delinsCGGCGGGGG
XR_928367.1:n.159+18_159+26delinsCGGCGGGGG
XR_928368.1:n.161+18_161+26delinsCGGCGGGGG
XM_011517384.3:c.118+18_118+26delinsCGGCGGGGG	XP_011515686.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013991.2:c.118+18_118+26delinsCGGCGGGGG	XP_016869480.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013992.2:c.118+18_118+26delinsCGGCGGGGG	XP_016869481.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013993.2:c.118+18_118+26delinsCGGCGGGGG	XP_016869482.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013994.2:c.118+18_118+26delinsCGGCGGGGG	XP_016869483.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013995.2:c.118+18_118+26delinsCGGCGGGGG	XP_016869484.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013996.2:c.118+18_118+26delinsCGGCGGGGG	XP_016869485.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013997.2:c.118+18_118+26delinsCGGCGGGGG	XP_016869486.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013998.1:c.118+18_118+26delinsCGGCGGGGG	XP_016869487.1:n.118+18_118+26delinsCGGCGGGGG
XM_017013999.2:c.118+18_118+26delinsCGGCGGGGG	XP_016869488.1:n.118+18_118+26delinsCGGCGGGGG
XR_001745626.2:n.155+18_155+26delinsCGGCGGGGG
XR_001745627.2:n.155+18_155+26delinsCGGCGGGGG
XR_001745628.2:n.155+18_155+26delinsCGGCGGGGG
XR_001745629.2:n.155+18_155+26delinsCGGCGGGGG
XR_001745630.2:n.155+18_155+26delinsCGGCGGGGG
NM_004260.4:c.118+18_118+26delinsCGGCGGGGG MANE Select	NP_004251.4:n.118+18_118+26delinsCGGCGGGGG