Canonical Allele Identifier: CA1539590460
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064725G= , CM000667.2:g.37064725G= GRCh38
NC_000005.9:g.37064827G= , CM000667.1:g.37064827G= GRCh37
NC_000005.8:g.37100584G= NCBI36
NG_006987.1:g.192843G=
NG_006987.2:g.192843G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8248G= (NIPBL) MANE Select ENSP00000282516.8:p.Glu2750=
ENST00000652901.1:c.*192G= (NIPBL) ENSP00000499536.1:n.*192G=
ENST00000282516.12:c.8248G= (NIPBL) ENSP00000282516.8:p.Glu2750=
ENST00000514335.1:n.2171G= (NIPBL)
ENST00000621733.1:c.148G= (NIPBL) ENSP00000480694.1:p.Glu50=
NM_015384.4:c.*702G= (NIPBL) NP_056199.2:n.*702G=
NM_133433.3:c.8248G= (NIPBL) NP_597677.2:p.Glu2750=
XM_005248280.2:c.*192G= (NIPBL) XP_005248337.1:n.*192G=
XM_005248282.3:c.7504G= (NIPBL) XP_005248339.2:p.Glu2502=
XM_006714467.2:c.8101G= (NIPBL) XP_006714530.1:p.Glu2701=
XM_006714468.1:c.8050G= (NIPBL) XP_006714531.1:p.Glu2684=
XM_011514014.1:c.7867G= (NIPBL) XP_011512316.1:p.Glu2623=
XM_005248280.3:c.*192G= (NIPBL) XP_005248337.1:n.*192G=
XM_005248282.5:c.7588G= (NIPBL) XP_005248339.3:p.Glu2530=
XM_006714468.2:c.8050G= (NIPBL) XP_006714531.1:p.Glu2684=
XM_017009329.1:c.*192G= (NIPBL) XP_016864818.1:n.*192G=
XM_017009330.2:c.6631G= (NIPBL) XP_016864819.1:p.Glu2211=
XM_017009331.1:c.6622G= (NIPBL) XP_016864820.1:p.Glu2208=
XR_925644.2:n.11957C= (CPLANE1)
NM_133433.4:c.8248G= (NIPBL) MANE Select NP_597677.2:p.Glu2750=
NM_015384.5:c.*702G= (NIPBL) NP_056199.2:n.*702G=