Canonical Allele Identifier: CA16616869
Gene: ZNF711 HGNC NCBI

Linked Data

ClinVar Variation Id: 417762
dbSNP Id: rs1060505033

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85264383T>C , CM000685.2:g.85264383T>C GRCh38
NC_000023.10:g.84519389T>C , CM000685.1:g.84519389T>C GRCh37
NC_000023.9:g.84406045T>C NCBI36
NG_012535.1:g.25393T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000674551.1:c.731T>C MANE Select ENSP00000502839.1:p.Ile244Thr
ENST00000276123.7:c.731T>C ENSP00000276123.3:p.Ile244Thr
ENST00000360700.4:c.731T>C ENSP00000353922.4:p.Ile244Thr
ENST00000373165.7:c.731T>C ENSP00000362260.3:p.Ile244Thr
NM_021998.4:c.731T>C NP_068838.3:p.Ile244Thr
XM_005262186.1:c.731T>C XP_005262243.1:p.Ile244Thr
XM_005262187.1:c.731T>C XP_005262244.1:p.Ile244Thr
XM_005262188.1:c.731T>C XP_005262245.1:p.Ile244Thr
XM_005262189.1:c.731T>C XP_005262246.1:p.Ile244Thr
XM_011531019.1:c.743T>C XP_011529321.1:p.Ile248Thr
XM_011531020.1:c.743T>C XP_011529322.1:p.Ile248Thr
XM_011531021.1:c.743T>C XP_011529323.1:p.Ile248Thr
XM_011531022.1:c.743T>C XP_011529324.1:p.Ile248Thr
XM_011531023.1:c.743T>C XP_011529325.1:p.Ile248Thr
XM_011531024.1:c.731T>C XP_011529326.1:p.Ile244Thr
XM_011531025.1:c.743T>C XP_011529327.1:p.Ile248Thr
XM_011531026.1:c.731T>C XP_011529328.1:p.Ile244Thr
NM_001330574.1:c.731T>C NP_001317503.1:p.Ile244Thr
XM_005262186.3:c.731T>C XP_005262243.1:p.Ile244Thr
XM_005262189.3:c.731T>C XP_005262246.1:p.Ile244Thr
XM_011531023.3:c.743T>C XP_011529325.1:p.Ile248Thr
XM_017029803.1:c.743T>C XP_016885292.1:p.Ile248Thr
XM_017029805.1:c.731T>C XP_016885294.1:p.Ile244Thr
XM_017029807.1:c.731T>C XP_016885296.1:p.Ile244Thr
XM_017029808.1:c.731T>C XP_016885297.1:p.Ile244Thr
XM_017029809.1:c.731T>C XP_016885298.1:p.Ile244Thr
NM_001330574.2:c.731T>C MANE Select NP_001317503.1:p.Ile244Thr
NM_001375431.1:c.731T>C NP_001362360.1:p.Ile244Thr
NM_001375432.1:c.731T>C NP_001362361.1:p.Ile244Thr
NM_001375433.1:c.731T>C NP_001362362.1:p.Ile244Thr
NM_001375434.1:c.731T>C NP_001362363.1:p.Ile244Thr
NM_001375435.1:c.731T>C NP_001362364.1:p.Ile244Thr
NM_001375436.1:c.731T>C NP_001362365.1:p.Ile244Thr
NM_001375437.1:c.731T>C NP_001362366.1:p.Ile244Thr
NM_021998.5:c.731T>C NP_068838.3:p.Ile244Thr