Canonical Allele Identifier: CA372685108

Gene: RECQL4

Linked Data

• ClinVar Variation Id: 647631
• ClinVar RCV Id: RCV000802182
• dbSNP Id: rs1586816517
• MyVariant Identifiers: chr8:g.145740624T>C (hg19) ; chr8:g.144515240T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144515240T>C , CM000670.2:g.144515240T>C	GRCh38
NC_000008.10:g.145740624T>C , CM000670.1:g.145740624T>C	GRCh37
NC_000008.9:g.145711432T>C	NCBI36
NG_016430.1:g.7587A>G
NG_033083.1:g.2276T>C
NG_016430.2:g.7587A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000688394.1:n.416A>G
ENST00000617875.6:c.1393A>G MANE Select	ENSP00000482313.2:p.Thr465Ala
ENST00000532846.2:c.278A>G
ENST00000617875.4:c.1393A>G	ENSP00000482313.1:p.Thr465Ala
ENST00000621189.4:c.322A>G	ENSP00000483145.1:p.Thr108Ala
NM_004260.3:c.1393A>G	NP_004251.3:p.Thr465Ala
XM_011517380.1:c.1393A>G	XP_011515682.1:p.Thr465Ala
XM_011517381.1:c.1297A>G	XP_011515683.1:p.Thr433Ala
XM_011517382.1:c.1393A>G	XP_011515684.1:p.Thr465Ala
XM_011517383.1:c.1393A>G	XP_011515685.1:p.Thr465Ala
XM_011517384.1:c.1393A>G	XP_011515686.1:p.Thr465Ala
XM_011517385.1:c.256A>G	XP_011515687.1:p.Thr86Ala
XR_928366.1:n.1434A>G
XR_928367.1:n.1434A>G
XR_928368.1:n.1436A>G
XM_011517384.3:c.1393A>G	XP_011515686.1:p.Thr465Ala
XM_017013991.2:c.1393A>G	XP_016869480.1:p.Thr465Ala
XM_017013992.2:c.1393A>G	XP_016869481.1:p.Thr465Ala
XM_017013993.2:c.1393A>G	XP_016869482.1:p.Thr465Ala
XM_017013994.2:c.1297A>G	XP_016869483.1:p.Thr433Ala
XM_017013995.2:c.1393A>G	XP_016869484.1:p.Thr465Ala
XM_017013996.2:c.1393A>G	XP_016869485.1:p.Thr465Ala
XM_017013997.2:c.1393A>G	XP_016869486.1:p.Thr465Ala
XM_017013998.1:c.1393A>G	XP_016869487.1:p.Thr465Ala
XM_017013999.2:c.1393A>G	XP_016869488.1:p.Thr465Ala
XM_017014000.1:c.256A>G	XP_016869489.1:p.Thr86Ala
XM_017014001.2:c.256A>G	XP_016869490.1:p.Thr86Ala
XR_001745626.2:n.1430A>G
XR_001745627.2:n.1430A>G
XR_001745628.2:n.1430A>G
XR_001745629.2:n.1430A>G
XR_001745630.2:n.1430A>G
NM_004260.4:c.1393A>G MANE Select	NP_004251.4:p.Thr465Ala