Canonical Allele Identifier: CA359522800
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064740G>C , CM000667.2:g.37064740G>C GRCh38
NC_000005.9:g.37064842G>C , CM000667.1:g.37064842G>C GRCh37
NC_000005.8:g.37100599G>C NCBI36
NG_006987.1:g.192858G>C
NG_006987.2:g.192858G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8263G>C (NIPBL) MANE Select ENSP00000282516.8:p.Asp2755His
ENST00000652901.1:c.*207G>C (NIPBL) ENSP00000499536.1:n.*207G>C
ENST00000282516.12:c.8263G>C (NIPBL) ENSP00000282516.8:p.Asp2755His
ENST00000514335.1:n.2186G>C (NIPBL)
ENST00000621733.1:c.163G>C (NIPBL) ENSP00000480694.1:p.Asp55His
NM_015384.4:c.*717G>C (NIPBL) NP_056199.2:n.*717G>C
NM_133433.3:c.8263G>C (NIPBL) NP_597677.2:p.Asp2755His
XM_005248280.2:c.*207G>C (NIPBL) XP_005248337.1:n.*207G>C
XM_005248282.3:c.7519G>C (NIPBL) XP_005248339.2:p.Asp2507His
XM_006714467.2:c.8116G>C (NIPBL) XP_006714530.1:p.Asp2706His
XM_006714468.1:c.8065G>C (NIPBL) XP_006714531.1:p.Asp2689His
XM_011514014.1:c.7882G>C (NIPBL) XP_011512316.1:p.Asp2628His
XM_005248280.3:c.*207G>C (NIPBL) XP_005248337.1:n.*207G>C
XM_005248282.5:c.7603G>C (NIPBL) XP_005248339.3:p.Asp2535His
XM_006714468.2:c.8065G>C (NIPBL) XP_006714531.1:p.Asp2689His
XM_017009329.1:c.*207G>C (NIPBL) XP_016864818.1:n.*207G>C
XM_017009330.2:c.6646G>C (NIPBL) XP_016864819.1:p.Asp2216His
XM_017009331.1:c.6637G>C (NIPBL) XP_016864820.1:p.Asp2213His
XR_925644.2:n.11942C>G (CPLANE1)
NM_133433.4:c.8263G>C (NIPBL) MANE Select NP_597677.2:p.Asp2755His
NM_015384.5:c.*717G>C (NIPBL) NP_056199.2:n.*717G>C