Canonical Allele Identifier: CA1826368063

Gene: RECQL4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144515092_144515093delinsGC , CM000670.2:g.144515092_144515093delinsGC	GRCh38
NC_000008.10:g.145740476_145740477delinsGC , CM000670.1:g.145740476_145740477delinsGC	GRCh37
NC_000008.9:g.145711284_145711285delinsGC	NCBI36
NG_016430.1:g.7734_7735delinsGC
NG_033083.1:g.2128_2129delinsGC
NG_016430.2:g.7734_7735delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688394.1:n.507-21_507-20delinsGC
ENST00000617875.6:c.1484-21_1484-20delinsGC MANE Select	ENSP00000482313.2:n.1484-21_1484-20delinsGC
ENST00000532846.2:c.369-51_369-50delinsGC
ENST00000617875.4:c.1484-21_1484-20delinsGC	ENSP00000482313.1:n.1484-21_1484-20delinsGC
ENST00000621189.4:c.413-21_413-20delinsGC	ENSP00000483145.1:n.413-21_413-20delinsGC
NM_004260.3:c.1484-21_1484-20delinsGC	NP_004251.3:n.1484-21_1484-20delinsGC
XM_011517380.1:c.1484-21_1484-20delinsGC	XP_011515682.1:n.1484-21_1484-20delinsGC
XM_011517381.1:c.1388-21_1388-20delinsGC	XP_011515683.1:n.1388-21_1388-20delinsGC
XM_011517382.1:c.1484-21_1484-20delinsGC	XP_011515684.1:n.1484-21_1484-20delinsGC
XM_011517383.1:c.1484-21_1484-20delinsGC	XP_011515685.1:n.1484-21_1484-20delinsGC
XM_011517384.1:c.1484-21_1484-20delinsGC	XP_011515686.1:n.1484-21_1484-20delinsGC
XM_011517385.1:c.347-21_347-20delinsGC	XP_011515687.1:n.347-21_347-20delinsGC
XR_928366.1:n.1525-21_1525-20delinsGC
XR_928367.1:n.1525-21_1525-20delinsGC
XR_928368.1:n.1527-21_1527-20delinsGC
XM_011517384.3:c.1484-21_1484-20delinsGC	XP_011515686.1:n.1484-21_1484-20delinsGC
XM_017013991.2:c.1484-21_1484-20delinsGC	XP_016869480.1:n.1484-21_1484-20delinsGC
XM_017013992.2:c.1484-21_1484-20delinsGC	XP_016869481.1:n.1484-21_1484-20delinsGC
XM_017013993.2:c.1484-21_1484-20delinsGC	XP_016869482.1:n.1484-21_1484-20delinsGC
XM_017013994.2:c.1388-21_1388-20delinsGC	XP_016869483.1:n.1388-21_1388-20delinsGC
XM_017013995.2:c.1484-21_1484-20delinsGC	XP_016869484.1:n.1484-21_1484-20delinsGC
XM_017013996.2:c.1484-21_1484-20delinsGC	XP_016869485.1:n.1484-21_1484-20delinsGC
XM_017013997.2:c.1484-21_1484-20delinsGC	XP_016869486.1:n.1484-21_1484-20delinsGC
XM_017013998.1:c.1484-21_1484-20delinsGC	XP_016869487.1:n.1484-21_1484-20delinsGC
XM_017013999.2:c.1484-21_1484-20delinsGC	XP_016869488.1:n.1484-21_1484-20delinsGC
XM_017014000.1:c.347-21_347-20delinsGC	XP_016869489.1:n.347-21_347-20delinsGC
XM_017014001.2:c.347-21_347-20delinsGC	XP_016869490.1:n.347-21_347-20delinsGC
XR_001745626.2:n.1521-21_1521-20delinsGC
XR_001745627.2:n.1521-21_1521-20delinsGC
XR_001745628.2:n.1521-21_1521-20delinsGC
XR_001745629.2:n.1521-21_1521-20delinsGC
XR_001745630.2:n.1521-21_1521-20delinsGC
NM_004260.4:c.1484-21_1484-20delinsGC MANE Select	NP_004251.4:n.1484-21_1484-20delinsGC