Canonical Allele Identifier: CA372687591

Gene: RECQL4

Linked Data

• MyVariant Identifiers: chr8:g.145741213G>C (hg19) ; chr8:g.144515829G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144515829G>C , CM000670.2:g.144515829G>C	GRCh38
NC_000008.10:g.145741213G>C , CM000670.1:g.145741213G>C	GRCh37
NC_000008.9:g.145712021G>C	NCBI36
NG_016430.1:g.6998C>G
NG_033083.1:g.2865G>C
NG_016430.2:g.6998C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617875.6:c.1193C>G MANE Select	ENSP00000482313.2:p.Thr398Arg
ENST00000532846.2:c.78C>G
ENST00000617875.4:c.1193C>G	ENSP00000482313.1:p.Thr398Arg
ENST00000621189.4:c.122C>G	ENSP00000483145.1:p.Thr41Arg
NM_004260.3:c.1193C>G	NP_004251.3:p.Thr398Arg
XM_011517380.1:c.1193C>G	XP_011515682.1:p.Thr398Arg
XM_011517381.1:c.1097C>G	XP_011515683.1:p.Thr366Arg
XM_011517382.1:c.1193C>G	XP_011515684.1:p.Thr398Arg
XM_011517383.1:c.1193C>G	XP_011515685.1:p.Thr398Arg
XM_011517384.1:c.1193C>G	XP_011515686.1:p.Thr398Arg
XM_011517385.1:c.60C>G	XP_011515687.1:p.His20Gln
XR_928366.1:n.1234C>G
XR_928367.1:n.1234C>G
XR_928368.1:n.1236C>G
XM_011517384.3:c.1193C>G	XP_011515686.1:p.Thr398Arg
XM_017013991.2:c.1193C>G	XP_016869480.1:p.Thr398Arg
XM_017013992.2:c.1193C>G	XP_016869481.1:p.Thr398Arg
XM_017013993.2:c.1193C>G	XP_016869482.1:p.Thr398Arg
XM_017013994.2:c.1097C>G	XP_016869483.1:p.Thr366Arg
XM_017013995.2:c.1193C>G	XP_016869484.1:p.Thr398Arg
XM_017013996.2:c.1193C>G	XP_016869485.1:p.Thr398Arg
XM_017013997.2:c.1193C>G	XP_016869486.1:p.Thr398Arg
XM_017013998.1:c.1193C>G	XP_016869487.1:p.Thr398Arg
XM_017013999.2:c.1193C>G	XP_016869488.1:p.Thr398Arg
XM_017014000.1:c.60C>G	XP_016869489.1:p.His20Gln
XM_017014001.2:c.60C>G	XP_016869490.1:p.His20Gln
XR_001745626.2:n.1230C>G
XR_001745627.2:n.1230C>G
XR_001745628.2:n.1230C>G
XR_001745629.2:n.1230C>G
XR_001745630.2:n.1230C>G
NM_004260.4:c.1193C>G MANE Select	NP_004251.4:p.Thr398Arg