Canonical Allele Identifier: CA372683642

Gene: RECQL4

Linked Data

• ClinVar Variation Id: 965416
• ClinVar RCV Id: RCV001239857
• dbSNP Id: rs1318317428
• gnomAD v4: 8-144514981-G-C
• MyVariant Identifiers: chr8:g.145740365G>C (hg19) ; chr8:g.144514981G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144514981G>C , CM000670.2:g.144514981G>C	GRCh38
NC_000008.10:g.145740365G>C , CM000670.1:g.145740365G>C	GRCh37
NC_000008.9:g.145711173G>C	NCBI36
NG_016430.1:g.7846C>G
NG_033083.1:g.2017G>C
NG_016430.2:g.7846C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688394.1:n.598C>G
ENST00000617875.6:c.1575C>G MANE Select	ENSP00000482313.2:p.Cys525Trp
ENST00000532846.2:c.430C>G
ENST00000617875.4:c.1575C>G	ENSP00000482313.1:p.Cys525Trp
ENST00000621189.4:c.504C>G	ENSP00000483145.1:p.Cys168Trp
NM_004260.3:c.1575C>G	NP_004251.3:p.Cys525Trp
XM_011517380.1:c.1575C>G	XP_011515682.1:p.Cys525Trp
XM_011517381.1:c.1479C>G	XP_011515683.1:p.Cys493Trp
XM_011517382.1:c.1575C>G	XP_011515684.1:p.Cys525Trp
XM_011517383.1:c.1575C>G	XP_011515685.1:p.Cys525Trp
XM_011517384.1:c.1575C>G	XP_011515686.1:p.Cys525Trp
XM_011517385.1:c.438C>G	XP_011515687.1:p.Cys146Trp
XR_928366.1:n.1616C>G
XR_928367.1:n.1616C>G
XR_928368.1:n.1618C>G
XM_011517384.3:c.1575C>G	XP_011515686.1:p.Cys525Trp
XM_017013991.2:c.1575C>G	XP_016869480.1:p.Cys525Trp
XM_017013992.2:c.1575C>G	XP_016869481.1:p.Cys525Trp
XM_017013993.2:c.1575C>G	XP_016869482.1:p.Cys525Trp
XM_017013994.2:c.1479C>G	XP_016869483.1:p.Cys493Trp
XM_017013995.2:c.1575C>G	XP_016869484.1:p.Cys525Trp
XM_017013996.2:c.1575C>G	XP_016869485.1:p.Cys525Trp
XM_017013997.2:c.1575C>G	XP_016869486.1:p.Cys525Trp
XM_017013998.1:c.1575C>G	XP_016869487.1:p.Cys525Trp
XM_017013999.2:c.1575C>G	XP_016869488.1:p.Cys525Trp
XM_017014000.1:c.438C>G	XP_016869489.1:p.Cys146Trp
XM_017014001.2:c.438C>G	XP_016869490.1:p.Cys146Trp
XR_001745626.2:n.1612C>G
XR_001745627.2:n.1612C>G
XR_001745628.2:n.1612C>G
XR_001745629.2:n.1612C>G
XR_001745630.2:n.1612C>G
NM_004260.4:c.1575C>G MANE Select	NP_004251.4:p.Cys525Trp