Canonical Allele Identifier: CA2689129023

Gene: RECQL4

Linked Data

• gnomAD v4: 8-144511905-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144511905A>G , CM000670.2:g.144511905A>G	GRCh38
NC_000008.10:g.145737288A>G , CM000670.1:g.145737288A>G	GRCh37
NC_000008.9:g.145708096A>G	NCBI36
NG_016430.1:g.10922T>C
NG_016430.2:g.10922T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617875.6:c.3393+6T>C MANE Select	ENSP00000482313.2:n.3393+6T>C
ENST00000301323.7:c.410+6T>C
ENST00000529424.2:n.50-116T>C
ENST00000531875.2:c.645T>C	ENSP00000477910.1:p.Ser215=
ENST00000617875.4:c.3393+6T>C	ENSP00000482313.1:n.3393+6T>C
ENST00000621189.4:c.2322+6T>C	ENSP00000483145.1:n.2322+6T>C
NM_004260.3:c.3393+6T>C	NP_004251.3:n.3393+6T>C
XM_011517380.1:c.3468+6T>C	XP_011515682.1:n.3468+6T>C
XM_011517381.1:c.3372+6T>C	XP_011515683.1:n.3372+6T>C
XM_011517382.1:c.3276+6T>C	XP_011515684.1:n.3276+6T>C
XM_011517383.1:c.3270+6T>C	XP_011515685.1:n.3270+6T>C
XM_011517384.1:c.3195+6T>C	XP_011515686.1:n.3195+6T>C
XM_011517385.1:c.2331+6T>C	XP_011515687.1:n.2331+6T>C
XR_928366.1:n.3353-116T>C
XR_928367.1:n.3448+6T>C
XR_928368.1:n.3341+6T>C
XM_011517384.3:c.3195+6T>C	XP_011515686.1:n.3195+6T>C
XM_017013991.2:c.3564T>C	XP_016869480.1:p.Ser1188=
XM_017013992.2:c.3489T>C	XP_016869481.1:p.Ser1163=
XM_017013993.2:c.3474T>C	XP_016869482.1:p.Ser1158=
XM_017013994.2:c.3468T>C	XP_016869483.1:p.Ser1156=
XM_017013995.2:c.3399T>C	XP_016869484.1:p.Ser1133=
XM_017013996.2:c.3558+6T>C	XP_016869485.1:n.3558+6T>C
XM_017013997.2:c.3366T>C	XP_016869486.1:p.Ser1122=
XM_017013998.1:c.3483+6T>C	XP_016869487.1:n.3483+6T>C
XM_017013999.2:c.3276T>C	XP_016869488.1:p.Ser1092=
XM_017014000.1:c.2427T>C	XP_016869489.1:p.Ser809=
XM_017014001.2:c.2337T>C	XP_016869490.1:p.Ser779=
XR_001745626.2:n.3439-116T>C
XR_001745627.2:n.3534+6T>C
XR_001745628.2:n.3425+6T>C
XR_001745629.2:n.3288+6T>C
XR_001745630.2:n.3090+6T>C
NM_004260.4:c.3393+6T>C MANE Select	NP_004251.4:n.3393+6T>C