Canonical Allele Identifier: CA6479085

Gene: RECQL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21486579G>A , CM000674.2:g.21486579G>A	GRCh38
NC_000012.11:g.21639513G>A , CM000674.1:g.21639513G>A	GRCh37
NC_000012.10:g.21530780G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002907.4:c.401C>T MANE Select	NP_002898.2:p.Thr134Ile
ENST00000444129.7:c.401C>T MANE Select	ENSP00000416739.2:p.Thr134Ile
NM_002907.3:c.401C>T	NP_002898.2:p.Thr134Ile
NM_032941.2:c.401C>T	NP_116559.1:p.Thr134Ile
NM_032941.3:c.401C>T	NP_116559.1:p.Thr134Ile
ENST00000314748.10:c.401C>T	ENSP00000318727.6:p.Thr134Ile
ENST00000396093.7:c.401C>T	ENSP00000379400.3:p.Thr134Ile
ENST00000421138.6:c.401C>T	ENSP00000395449.2:p.Thr134Ile
ENST00000444129.6:c.401C>T	ENSP00000416739.2:p.Thr134Ile
XM_005253461.3:c.401C>T	XP_005253518.1:p.Thr134Ile
XM_005253462.3:c.401C>T	XP_005253519.1:p.Thr134Ile
XM_005253462.5:c.401C>T	XP_005253519.1:p.Thr134Ile
XM_005253463.2:c.401C>T	XP_005253520.1:p.Thr134Ile
XM_005253463.4:c.401C>T	XP_005253520.1:p.Thr134Ile
XM_005253464.2:c.401C>T	XP_005253521.1:p.Thr134Ile
XM_005253464.4:c.401C>T	XP_005253521.1:p.Thr134Ile
XM_006719133.2:c.401C>T	XP_006719196.1:p.Thr134Ile
XM_011520811.1:c.401C>T	XP_011519113.1:p.Thr134Ile