Canonical Allele Identifier: CA2689128767

Gene: RECQL4

Linked Data

• gnomAD v4: 8-144511831-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144511831G>A , CM000670.2:g.144511831G>A	GRCh38
NC_000008.10:g.145737214G>A , CM000670.1:g.145737214G>A	GRCh37
NC_000008.9:g.145708022G>A	NCBI36
NG_016430.1:g.10996C>T
NG_016430.2:g.10996C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617875.6:c.3394-42C>T MANE Select	ENSP00000482313.2:n.3394-42C>T
ENST00000301323.7:c.411-42C>T
ENST00000529424.2:n.50-42C>T
ENST00000531875.2:c.649-42C>T	ENSP00000477910.1:n.649-42C>T
ENST00000617875.4:c.3394-42C>T	ENSP00000482313.1:n.3394-42C>T
ENST00000621189.4:c.2323-42C>T	ENSP00000483145.1:n.2323-42C>T
NM_004260.3:c.3394-42C>T	NP_004251.3:n.3394-42C>T
XM_011517380.1:c.3469-42C>T	XP_011515682.1:n.3469-42C>T
XM_011517381.1:c.3373-42C>T	XP_011515683.1:n.3373-42C>T
XM_011517382.1:c.3277-42C>T	XP_011515684.1:n.3277-42C>T
XM_011517383.1:c.3271-42C>T	XP_011515685.1:n.3271-42C>T
XM_011517384.1:c.3196-42C>T	XP_011515686.1:n.3196-42C>T
XM_011517385.1:c.2332-42C>T	XP_011515687.1:n.2332-42C>T
XR_928366.1:n.3353-42C>T
XR_928367.1:n.3449-42C>T
XR_928368.1:n.3342-42C>T
XM_011517384.3:c.3196-42C>T	XP_011515686.1:n.3196-42C>T
XM_017013991.2:c.3638C>T	XP_016869480.1:p.Ala1213Val
XM_017013992.2:c.3563C>T	XP_016869481.1:p.Ala1188Val
XM_017013993.2:c.3548C>T	XP_016869482.1:p.Ala1183Val
XM_017013994.2:c.3542C>T	XP_016869483.1:p.Ala1181Val
XM_017013995.2:c.3473C>T	XP_016869484.1:p.Ala1158Val
XM_017013996.2:c.3559-42C>T	XP_016869485.1:n.3559-42C>T
XM_017013997.2:c.3440C>T	XP_016869486.1:p.Ala1147Val
XM_017013998.1:c.3484-42C>T	XP_016869487.1:n.3484-42C>T
XM_017013999.2:c.3350C>T	XP_016869488.1:p.Ala1117Val
XM_017014000.1:c.2501C>T	XP_016869489.1:p.Ala834Val
XM_017014001.2:c.2411C>T	XP_016869490.1:p.Ala804Val
XR_001745626.2:n.3439-42C>T
XR_001745627.2:n.3535-42C>T
XR_001745628.2:n.3426-42C>T
XR_001745629.2:n.3289-42C>T
XR_001745630.2:n.3091-42C>T
NM_004260.4:c.3394-42C>T MANE Select	NP_004251.4:n.3394-42C>T