Canonical Allele Identifier: CA1826368169
Gene: RECQL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144515239_144515241delinsGTC , CM000670.2:g.144515239_144515241delinsGTC GRCh38
NC_000008.10:g.145740623_145740625delinsGTC , CM000670.1:g.145740623_145740625delinsGTC GRCh37
NC_000008.9:g.145711431_145711433delinsGTC NCBI36
NG_016430.1:g.7586_7588delinsGAC
NG_033083.1:g.2275_2277delinsGTC
NG_016430.2:g.7586_7588delinsGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000688394.1:n.415_417delinsGAC
ENST00000617875.6:c.1392_1394delinsGAC MANE Select ENSP00000482313.2:p.Glu464=
ENST00000532846.2:c.277_279delinsGAC
ENST00000617875.4:c.1392_1394delinsGAC ENSP00000482313.1:p.Glu464=
ENST00000621189.4:c.321_323delinsGAC ENSP00000483145.1:p.Glu107=
NM_004260.3:c.1392_1394delinsGAC NP_004251.3:p.Glu464=
XM_011517380.1:c.1392_1394delinsGAC XP_011515682.1:p.Glu464=
XM_011517381.1:c.1296_1298delinsGAC XP_011515683.1:p.Glu432=
XM_011517382.1:c.1392_1394delinsGAC XP_011515684.1:p.Glu464=
XM_011517383.1:c.1392_1394delinsGAC XP_011515685.1:p.Glu464=
XM_011517384.1:c.1392_1394delinsGAC XP_011515686.1:p.Glu464=
XM_011517385.1:c.255_257delinsGAC XP_011515687.1:p.Glu85=
XR_928366.1:n.1433_1435delinsGAC
XR_928367.1:n.1433_1435delinsGAC
XR_928368.1:n.1435_1437delinsGAC
XM_011517384.3:c.1392_1394delinsGAC XP_011515686.1:p.Glu464=
XM_017013991.2:c.1392_1394delinsGAC XP_016869480.1:p.Glu464=
XM_017013992.2:c.1392_1394delinsGAC XP_016869481.1:p.Glu464=
XM_017013993.2:c.1392_1394delinsGAC XP_016869482.1:p.Glu464=
XM_017013994.2:c.1296_1298delinsGAC XP_016869483.1:p.Glu432=
XM_017013995.2:c.1392_1394delinsGAC XP_016869484.1:p.Glu464=
XM_017013996.2:c.1392_1394delinsGAC XP_016869485.1:p.Glu464=
XM_017013997.2:c.1392_1394delinsGAC XP_016869486.1:p.Glu464=
XM_017013998.1:c.1392_1394delinsGAC XP_016869487.1:p.Glu464=
XM_017013999.2:c.1392_1394delinsGAC XP_016869488.1:p.Glu464=
XM_017014000.1:c.255_257delinsGAC XP_016869489.1:p.Glu85=
XM_017014001.2:c.255_257delinsGAC XP_016869490.1:p.Glu85=
XR_001745626.2:n.1429_1431delinsGAC
XR_001745627.2:n.1429_1431delinsGAC
XR_001745628.2:n.1429_1431delinsGAC
XR_001745629.2:n.1429_1431delinsGAC
XR_001745630.2:n.1429_1431delinsGAC
NM_004260.4:c.1392_1394delinsGAC MANE Select NP_004251.4:p.Glu464=