Canonical Allele Identifier: CA187687991
Gene: RECQL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 529095
ClinVar RCV Id: RCV001437570
dbSNP Id: rs1002397552

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144515834T>C , CM000670.2:g.144515834T>C GRCh38
NC_000008.10:g.145741218T>C , CM000670.1:g.145741218T>C GRCh37
NC_000008.9:g.145712026T>C NCBI36
NG_016430.1:g.6993A>G
NG_033083.1:g.2870T>C
NG_016430.2:g.6993A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000617875.6:c.1188A>G MANE Select ENSP00000482313.2:p.Thr396=
ENST00000532846.2:c.73A>G
ENST00000617875.4:c.1188A>G ENSP00000482313.1:p.Thr396=
ENST00000621189.4:c.117A>G ENSP00000483145.1:p.Thr39=
NM_004260.3:c.1188A>G NP_004251.3:p.Thr396=
XM_011517380.1:c.1188A>G XP_011515682.1:p.Thr396=
XM_011517381.1:c.1092A>G XP_011515683.1:p.Thr364=
XM_011517382.1:c.1188A>G XP_011515684.1:p.Thr396=
XM_011517383.1:c.1188A>G XP_011515685.1:p.Thr396=
XM_011517384.1:c.1188A>G XP_011515686.1:p.Thr396=
XM_011517385.1:c.55A>G XP_011515687.1:p.Ser19Gly
XR_928366.1:n.1229A>G
XR_928367.1:n.1229A>G
XR_928368.1:n.1231A>G
XM_011517384.3:c.1188A>G XP_011515686.1:p.Thr396=
XM_017013991.2:c.1188A>G XP_016869480.1:p.Thr396=
XM_017013992.2:c.1188A>G XP_016869481.1:p.Thr396=
XM_017013993.2:c.1188A>G XP_016869482.1:p.Thr396=
XM_017013994.2:c.1092A>G XP_016869483.1:p.Thr364=
XM_017013995.2:c.1188A>G XP_016869484.1:p.Thr396=
XM_017013996.2:c.1188A>G XP_016869485.1:p.Thr396=
XM_017013997.2:c.1188A>G XP_016869486.1:p.Thr396=
XM_017013998.1:c.1188A>G XP_016869487.1:p.Thr396=
XM_017013999.2:c.1188A>G XP_016869488.1:p.Thr396=
XM_017014000.1:c.55A>G XP_016869489.1:p.Ser19Gly
XM_017014001.2:c.55A>G XP_016869490.1:p.Ser19Gly
XR_001745626.2:n.1225A>G
XR_001745627.2:n.1225A>G
XR_001745628.2:n.1225A>G
XR_001745629.2:n.1225A>G
XR_001745630.2:n.1225A>G
NM_004260.4:c.1188A>G MANE Select NP_004251.4:p.Thr396=