Canonical Allele Identifier: CA1539590781
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064859C= , CM000667.2:g.37064859C= GRCh38
NC_000005.9:g.37064961C= , CM000667.1:g.37064961C= GRCh37
NC_000005.8:g.37100718C= NCBI36
NG_006987.1:g.192977C=
NG_006987.2:g.192977C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.8382C= (NIPBL) MANE Select ENSP00000282516.8:p.Ser2794=
ENST00000652901.1:c.*326C= (NIPBL) ENSP00000499536.1:n.*326C=
ENST00000282516.12:c.8382C= (NIPBL) ENSP00000282516.8:p.Ser2794=
ENST00000514335.1:n.2305C= (NIPBL)
ENST00000621733.1:c.282C= (NIPBL) ENSP00000480694.1:p.Ser94=
NM_015384.4:c.*836C= (NIPBL) NP_056199.2:n.*836C=
NM_133433.3:c.8382C= (NIPBL) NP_597677.2:p.Ser2794=
XM_005248280.2:c.*326C= (NIPBL) XP_005248337.1:n.*326C=
XM_005248282.3:c.7638C= (NIPBL) XP_005248339.2:p.Ser2546=
XM_006714467.2:c.8235C= (NIPBL) XP_006714530.1:p.Ser2745=
XM_006714468.1:c.8184C= (NIPBL) XP_006714531.1:p.Ser2728=
XM_011514014.1:c.8001C= (NIPBL) XP_011512316.1:p.Ser2667=
XM_005248280.3:c.*326C= (NIPBL) XP_005248337.1:n.*326C=
XM_005248282.5:c.7722C= (NIPBL) XP_005248339.3:p.Ser2574=
XM_006714468.2:c.8184C= (NIPBL) XP_006714531.1:p.Ser2728=
XM_017009329.1:c.*326C= (NIPBL) XP_016864818.1:n.*326C=
XM_017009330.2:c.6765C= (NIPBL) XP_016864819.1:p.Ser2255=
XM_017009331.1:c.6756C= (NIPBL) XP_016864820.1:p.Ser2252=
XR_925644.2:n.11823G= (CPLANE1)
NM_133433.4:c.8382C= (NIPBL) MANE Select NP_597677.2:p.Ser2794=
NM_015384.5:c.*836C= (NIPBL) NP_056199.2:n.*836C=