Canonical Allele Identifier: CA2689136305

Gene: RECQL4

Linked Data

• gnomAD v4: 8-144515695-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144515695_144515696insA , CM000670.2:g.144515695_144515696insA	GRCh38
NC_000008.10:g.145741079_145741080insA , CM000670.1:g.145741079_145741080insA	GRCh37
NC_000008.9:g.145711887_145711888insA	NCBI36
NG_016430.1:g.7131_7132insT
NG_033083.1:g.2731_2732insA
NG_016430.2:g.7131_7132insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688394.1:n.43_44insT
ENST00000617875.6:c.1258+68_1258+69insT MANE Select	ENSP00000482313.2:n.1258+68_1258+69insT
ENST00000532846.2:c.143+68_143+69insT
ENST00000617875.4:c.1258+68_1258+69insT	ENSP00000482313.1:n.1258+68_1258+69insT
ENST00000621189.4:c.187+68_187+69insT	ENSP00000483145.1:n.187+68_187+69insT
NM_004260.3:c.1258+68_1258+69insT	NP_004251.3:n.1258+68_1258+69insT
XM_011517380.1:c.1258+68_1258+69insT	XP_011515682.1:n.1258+68_1258+69insT
XM_011517381.1:c.1162+68_1162+69insT	XP_011515683.1:n.1162+68_1162+69insT
XM_011517382.1:c.1258+68_1258+69insT	XP_011515684.1:n.1258+68_1258+69insT
XM_011517383.1:c.1258+68_1258+69insT	XP_011515685.1:n.1258+68_1258+69insT
XM_011517384.1:c.1258+68_1258+69insT	XP_011515686.1:n.1258+68_1258+69insT
XM_011517385.1:c.125+68_125+69insT	XP_011515687.1:n.125+68_125+69insT
XR_928366.1:n.1299+68_1299+69insT
XR_928367.1:n.1299+68_1299+69insT
XR_928368.1:n.1301+68_1301+69insT
XM_011517384.3:c.1258+68_1258+69insT	XP_011515686.1:n.1258+68_1258+69insT
XM_017013991.2:c.1258+68_1258+69insT	XP_016869480.1:n.1258+68_1258+69insT
XM_017013992.2:c.1258+68_1258+69insT	XP_016869481.1:n.1258+68_1258+69insT
XM_017013993.2:c.1258+68_1258+69insT	XP_016869482.1:n.1258+68_1258+69insT
XM_017013994.2:c.1162+68_1162+69insT	XP_016869483.1:n.1162+68_1162+69insT
XM_017013995.2:c.1258+68_1258+69insT	XP_016869484.1:n.1258+68_1258+69insT
XM_017013996.2:c.1258+68_1258+69insT	XP_016869485.1:n.1258+68_1258+69insT
XM_017013997.2:c.1258+68_1258+69insT	XP_016869486.1:n.1258+68_1258+69insT
XM_017013998.1:c.1258+68_1258+69insT	XP_016869487.1:n.1258+68_1258+69insT
XM_017013999.2:c.1258+68_1258+69insT	XP_016869488.1:n.1258+68_1258+69insT
XM_017014000.1:c.125+68_125+69insT	XP_016869489.1:n.125+68_125+69insT
XM_017014001.2:c.125+68_125+69insT	XP_016869490.1:n.125+68_125+69insT
XR_001745626.2:n.1295+68_1295+69insT
XR_001745627.2:n.1295+68_1295+69insT
XR_001745628.2:n.1295+68_1295+69insT
XR_001745629.2:n.1295+68_1295+69insT
XR_001745630.2:n.1295+68_1295+69insT
NM_004260.4:c.1258+68_1258+69insT MANE Select	NP_004251.4:n.1258+68_1258+69insT