Canonical Allele Identifier: CA1539590221
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064610C= , CM000667.2:g.37064610C= GRCh38
NC_000005.9:g.37064712C= , CM000667.1:g.37064712C= GRCh37
NC_000005.8:g.37100469C= NCBI36
NG_006987.1:g.192728C=
NG_006987.2:g.192728C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8133C= (NIPBL) MANE Select ENSP00000282516.8:p.Ile2711=
ENST00000652901.1:c.*77C= (NIPBL) ENSP00000499536.1:n.*77C=
ENST00000282516.12:c.8133C= (NIPBL) ENSP00000282516.8:p.Ile2711=
ENST00000514335.1:n.2056C= (NIPBL)
ENST00000621733.1:c.33C= (NIPBL) ENSP00000480694.1:p.Ile11=
NM_015384.4:c.*587C= (NIPBL) NP_056199.2:n.*587C=
NM_133433.3:c.8133C= (NIPBL) NP_597677.2:p.Ile2711=
XM_005248280.2:c.*77C= (NIPBL) XP_005248337.1:n.*77C=
XM_005248282.3:c.7389C= (NIPBL) XP_005248339.2:p.Ile2463=
XM_006714467.2:c.7986C= (NIPBL) XP_006714530.1:p.Ile2662=
XM_006714468.1:c.7935C= (NIPBL) XP_006714531.1:p.Ile2645=
XM_011514014.1:c.7752C= (NIPBL) XP_011512316.1:p.Ile2584=
XM_005248280.3:c.*77C= (NIPBL) XP_005248337.1:n.*77C=
XM_005248282.5:c.7473C= (NIPBL) XP_005248339.3:p.Ile2491=
XM_006714468.2:c.7935C= (NIPBL) XP_006714531.1:p.Ile2645=
XM_017009329.1:c.*77C= (NIPBL) XP_016864818.1:n.*77C=
XM_017009330.2:c.6516C= (NIPBL) XP_016864819.1:p.Ile2172=
XM_017009331.1:c.6507C= (NIPBL) XP_016864820.1:p.Ile2169=
XR_925644.2:n.12072G= (CPLANE1)
NM_133433.4:c.8133C= (NIPBL) MANE Select NP_597677.2:p.Ile2711=
NM_015384.5:c.*587C= (NIPBL) NP_056199.2:n.*587C=