Canonical Allele Identifier: CA2689128856

Gene: RECQL4

Linked Data

• gnomAD v4: 8-144511861-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144511861G>A , CM000670.2:g.144511861G>A	GRCh38
NC_000008.10:g.145737244G>A , CM000670.1:g.145737244G>A	GRCh37
NC_000008.9:g.145708052G>A	NCBI36
NG_016430.1:g.10966C>T
NG_016430.2:g.10966C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617875.6:c.3393+50C>T MANE Select	ENSP00000482313.2:n.3393+50C>T
ENST00000301323.7:c.410+50C>T
ENST00000529424.2:n.50-72C>T
ENST00000531875.2:c.648+41C>T	ENSP00000477910.1:n.648+41C>T
ENST00000617875.4:c.3393+50C>T	ENSP00000482313.1:n.3393+50C>T
ENST00000621189.4:c.2322+50C>T	ENSP00000483145.1:n.2322+50C>T
NM_004260.3:c.3393+50C>T	NP_004251.3:n.3393+50C>T
XM_011517380.1:c.3468+50C>T	XP_011515682.1:n.3468+50C>T
XM_011517381.1:c.3372+50C>T	XP_011515683.1:n.3372+50C>T
XM_011517382.1:c.3276+50C>T	XP_011515684.1:n.3276+50C>T
XM_011517383.1:c.3270+50C>T	XP_011515685.1:n.3270+50C>T
XM_011517384.1:c.3195+50C>T	XP_011515686.1:n.3195+50C>T
XM_011517385.1:c.2331+50C>T	XP_011515687.1:n.2331+50C>T
XR_928366.1:n.3353-72C>T
XR_928367.1:n.3448+50C>T
XR_928368.1:n.3341+50C>T
XM_011517384.3:c.3195+50C>T	XP_011515686.1:n.3195+50C>T
XM_017013991.2:c.3608C>T	XP_016869480.1:p.Ala1203Val
XM_017013992.2:c.3533C>T	XP_016869481.1:p.Ala1178Val
XM_017013993.2:c.3518C>T	XP_016869482.1:p.Ala1173Val
XM_017013994.2:c.3512C>T	XP_016869483.1:p.Ala1171Val
XM_017013995.2:c.3443C>T	XP_016869484.1:p.Ala1148Val
XM_017013996.2:c.3558+50C>T	XP_016869485.1:n.3558+50C>T
XM_017013997.2:c.3410C>T	XP_016869486.1:p.Ala1137Val
XM_017013998.1:c.3483+50C>T	XP_016869487.1:n.3483+50C>T
XM_017013999.2:c.3320C>T	XP_016869488.1:p.Ala1107Val
XM_017014000.1:c.2471C>T	XP_016869489.1:p.Ala824Val
XM_017014001.2:c.2381C>T	XP_016869490.1:p.Ala794Val
XR_001745626.2:n.3439-72C>T
XR_001745627.2:n.3534+50C>T
XR_001745628.2:n.3425+50C>T
XR_001745629.2:n.3288+50C>T
XR_001745630.2:n.3090+50C>T
NM_004260.4:c.3393+50C>T MANE Select	NP_004251.4:n.3393+50C>T