Canonical Allele Identifier: CA2580078779

Gene: RECQL4

Linked Data

• ClinVar Variation Id: 2011737
• ClinVar RCV Id: RCV002838633

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144511893T>A , CM000670.2:g.144511893T>A	GRCh38
NC_000008.10:g.145737276T>A , CM000670.1:g.145737276T>A	GRCh37
NC_000008.9:g.145708084T>A	NCBI36
NG_016430.1:g.10934A>T
NG_016430.2:g.10934A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617875.6:c.3393+18A>T MANE Select	ENSP00000482313.2:n.3393+18A>T
ENST00000301323.7:c.410+18A>T
ENST00000529424.2:n.50-104A>T
ENST00000531875.2:c.648+9A>T	ENSP00000477910.1:n.648+9A>T
ENST00000617875.4:c.3393+18A>T	ENSP00000482313.1:n.3393+18A>T
ENST00000621189.4:c.2322+18A>T	ENSP00000483145.1:n.2322+18A>T
NM_004260.3:c.3393+18A>T	NP_004251.3:n.3393+18A>T
XM_011517380.1:c.3468+18A>T	XP_011515682.1:n.3468+18A>T
XM_011517381.1:c.3372+18A>T	XP_011515683.1:n.3372+18A>T
XM_011517382.1:c.3276+18A>T	XP_011515684.1:n.3276+18A>T
XM_011517383.1:c.3270+18A>T	XP_011515685.1:n.3270+18A>T
XM_011517384.1:c.3195+18A>T	XP_011515686.1:n.3195+18A>T
XM_011517385.1:c.2331+18A>T	XP_011515687.1:n.2331+18A>T
XR_928366.1:n.3353-104A>T
XR_928367.1:n.3448+18A>T
XR_928368.1:n.3341+18A>T
XM_011517384.3:c.3195+18A>T	XP_011515686.1:n.3195+18A>T
XM_017013991.2:c.3576A>T	XP_016869480.1:p.Pro1192=
XM_017013992.2:c.3501A>T	XP_016869481.1:p.Pro1167=
XM_017013993.2:c.3486A>T	XP_016869482.1:p.Pro1162=
XM_017013994.2:c.3480A>T	XP_016869483.1:p.Pro1160=
XM_017013995.2:c.3411A>T	XP_016869484.1:p.Pro1137=
XM_017013996.2:c.3558+18A>T	XP_016869485.1:n.3558+18A>T
XM_017013997.2:c.3378A>T	XP_016869486.1:p.Pro1126=
XM_017013998.1:c.3483+18A>T	XP_016869487.1:n.3483+18A>T
XM_017013999.2:c.3288A>T	XP_016869488.1:p.Pro1096=
XM_017014000.1:c.2439A>T	XP_016869489.1:p.Pro813=
XM_017014001.2:c.2349A>T	XP_016869490.1:p.Pro783=
XR_001745626.2:n.3439-104A>T
XR_001745627.2:n.3534+18A>T
XR_001745628.2:n.3425+18A>T
XR_001745629.2:n.3288+18A>T
XR_001745630.2:n.3090+18A>T
NM_004260.4:c.3393+18A>T MANE Select	NP_004251.4:n.3393+18A>T