Canonical Allele Identifier: CA359522424
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064653A>G , CM000667.2:g.37064653A>G GRCh38
NC_000005.9:g.37064755A>G , CM000667.1:g.37064755A>G GRCh37
NC_000005.8:g.37100512A>G NCBI36
NG_006987.1:g.192771A>G
NG_006987.2:g.192771A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8176A>G (NIPBL) MANE Select ENSP00000282516.8:p.Arg2726Gly
ENST00000652901.1:c.*120A>G (NIPBL) ENSP00000499536.1:n.*120A>G
ENST00000282516.12:c.8176A>G (NIPBL) ENSP00000282516.8:p.Arg2726Gly
ENST00000514335.1:n.2099A>G (NIPBL)
ENST00000621733.1:c.76A>G (NIPBL) ENSP00000480694.1:p.Arg26Gly
NM_015384.4:c.*630A>G (NIPBL) NP_056199.2:n.*630A>G
NM_133433.3:c.8176A>G (NIPBL) NP_597677.2:p.Arg2726Gly
XM_005248280.2:c.*120A>G (NIPBL) XP_005248337.1:n.*120A>G
XM_005248282.3:c.7432A>G (NIPBL) XP_005248339.2:p.Arg2478Gly
XM_006714467.2:c.8029A>G (NIPBL) XP_006714530.1:p.Arg2677Gly
XM_006714468.1:c.7978A>G (NIPBL) XP_006714531.1:p.Arg2660Gly
XM_011514014.1:c.7795A>G (NIPBL) XP_011512316.1:p.Arg2599Gly
XM_005248280.3:c.*120A>G (NIPBL) XP_005248337.1:n.*120A>G
XM_005248282.5:c.7516A>G (NIPBL) XP_005248339.3:p.Arg2506Gly
XM_006714468.2:c.7978A>G (NIPBL) XP_006714531.1:p.Arg2660Gly
XM_017009329.1:c.*120A>G (NIPBL) XP_016864818.1:n.*120A>G
XM_017009330.2:c.6559A>G (NIPBL) XP_016864819.1:p.Arg2187Gly
XM_017009331.1:c.6550A>G (NIPBL) XP_016864820.1:p.Arg2184Gly
XR_925644.2:n.12029T>C (CPLANE1)
NM_133433.4:c.8176A>G (NIPBL) MANE Select NP_597677.2:p.Arg2726Gly
NM_015384.5:c.*630A>G (NIPBL) NP_056199.2:n.*630A>G