Canonical Allele Identifier: CA1826368443

Gene: RECQL4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144515606_144515609delinsATCG , CM000670.2:g.144515606_144515609delinsATCG	GRCh38
NC_000008.10:g.145740990_145740993delinsATCG , CM000670.1:g.145740990_145740993delinsATCG	GRCh37
NC_000008.9:g.145711798_145711801delinsATCG	NCBI36
NG_016430.1:g.7218_7221delinsCGAT
NG_033083.1:g.2642_2645delinsATCG
NG_016430.2:g.7218_7221delinsCGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688394.1:n.130_133delinsCGAT
ENST00000617875.6:c.1259-152_1259-149delinsCGAT MANE Select	ENSP00000482313.2:n.1259-152_1259-149delinsCGAT
ENST00000532846.2:c.144-152_144-149delinsCGAT
ENST00000617875.4:c.1259-152_1259-149delinsCGAT	ENSP00000482313.1:n.1259-152_1259-149delinsCGAT
ENST00000621189.4:c.188-152_188-149delinsCGAT	ENSP00000483145.1:n.188-152_188-149delinsCGAT
NM_004260.3:c.1259-152_1259-149delinsCGAT	NP_004251.3:n.1259-152_1259-149delinsCGAT
XM_011517380.1:c.1259-152_1259-149delinsCGAT	XP_011515682.1:n.1259-152_1259-149delinsCGAT
XM_011517381.1:c.1163-152_1163-149delinsCGAT	XP_011515683.1:n.1163-152_1163-149delinsCGAT
XM_011517382.1:c.1259-152_1259-149delinsCGAT	XP_011515684.1:n.1259-152_1259-149delinsCGAT
XM_011517383.1:c.1259-152_1259-149delinsCGAT	XP_011515685.1:n.1259-152_1259-149delinsCGAT
XM_011517384.1:c.1259-152_1259-149delinsCGAT	XP_011515686.1:n.1259-152_1259-149delinsCGAT
XM_011517385.1:c.126-156_126-153delinsCGAT	XP_011515687.1:n.126-156_126-153delinsCGAT
XR_928366.1:n.1300-152_1300-149delinsCGAT
XR_928367.1:n.1300-152_1300-149delinsCGAT
XR_928368.1:n.1302-152_1302-149delinsCGAT
XM_011517384.3:c.1259-152_1259-149delinsCGAT	XP_011515686.1:n.1259-152_1259-149delinsCGAT
XM_017013991.2:c.1259-152_1259-149delinsCGAT	XP_016869480.1:n.1259-152_1259-149delinsCGAT
XM_017013992.2:c.1259-152_1259-149delinsCGAT	XP_016869481.1:n.1259-152_1259-149delinsCGAT
XM_017013993.2:c.1259-152_1259-149delinsCGAT	XP_016869482.1:n.1259-152_1259-149delinsCGAT
XM_017013994.2:c.1163-152_1163-149delinsCGAT	XP_016869483.1:n.1163-152_1163-149delinsCGAT
XM_017013995.2:c.1259-152_1259-149delinsCGAT	XP_016869484.1:n.1259-152_1259-149delinsCGAT
XM_017013996.2:c.1259-152_1259-149delinsCGAT	XP_016869485.1:n.1259-152_1259-149delinsCGAT
XM_017013997.2:c.1259-152_1259-149delinsCGAT	XP_016869486.1:n.1259-152_1259-149delinsCGAT
XM_017013998.1:c.1259-152_1259-149delinsCGAT	XP_016869487.1:n.1259-152_1259-149delinsCGAT
XM_017013999.2:c.1259-152_1259-149delinsCGAT	XP_016869488.1:n.1259-152_1259-149delinsCGAT
XM_017014000.1:c.126-156_126-153delinsCGAT	XP_016869489.1:n.126-156_126-153delinsCGAT
XM_017014001.2:c.126-156_126-153delinsCGAT	XP_016869490.1:n.126-156_126-153delinsCGAT
XR_001745626.2:n.1296-152_1296-149delinsCGAT
XR_001745627.2:n.1296-152_1296-149delinsCGAT
XR_001745628.2:n.1296-152_1296-149delinsCGAT
XR_001745629.2:n.1296-152_1296-149delinsCGAT
XR_001745630.2:n.1296-152_1296-149delinsCGAT
NM_004260.4:c.1259-152_1259-149delinsCGAT MANE Select	NP_004251.4:n.1259-152_1259-149delinsCGAT