Canonical Allele Identifier: CA1539589694
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064358G= , CM000667.2:g.37064358G= GRCh38
NC_000005.9:g.37064460G= , CM000667.1:g.37064460G= GRCh37
NC_000005.8:g.37100217G= NCBI36
NG_006987.1:g.192476G=
NG_006987.2:g.192476G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8050-169G= (NIPBL) MANE Select ENSP00000282516.8:n.8050-169G=
ENST00000652901.1:c.7944-169G= (NIPBL) ENSP00000499536.1:n.7944-169G=
ENST00000282516.12:c.8050-169G= (NIPBL) ENSP00000282516.8:n.8050-169G=
ENST00000514335.1:n.1973-169G= (NIPBL)
ENST00000621733.1:c.1-220G= (NIPBL) ENSP00000480694.1:n.1-220G=
NM_015384.4:c.*335G= (NIPBL) NP_056199.2:n.*335G=
NM_133433.3:c.8050-169G= (NIPBL) NP_597677.2:n.8050-169G=
XM_005248280.2:c.8091-169G= (NIPBL) XP_005248337.1:n.8091-169G=
XM_005248282.3:c.7306-169G= (NIPBL) XP_005248339.2:n.7306-169G=
XM_006714467.2:c.7903-169G= (NIPBL) XP_006714530.1:n.7903-169G=
XM_006714468.1:c.7852-169G= (NIPBL) XP_006714531.1:n.7852-169G=
XM_011514014.1:c.7669-169G= (NIPBL) XP_011512316.1:n.7669-169G=
XM_005248280.3:c.8091-169G= (NIPBL) XP_005248337.1:n.8091-169G=
XM_005248282.5:c.7390-169G= (NIPBL) XP_005248339.3:n.7390-169G=
XM_006714468.2:c.7852-169G= (NIPBL) XP_006714531.1:n.7852-169G=
XM_017009329.1:c.7944-169G= (NIPBL) XP_016864818.1:n.7944-169G=
XM_017009330.2:c.6433-169G= (NIPBL) XP_016864819.1:n.6433-169G=
XM_017009331.1:c.6424-169G= (NIPBL) XP_016864820.1:n.6424-169G=
XR_925644.2:n.12324C= (CPLANE1)
NM_133433.4:c.8050-169G= (NIPBL) MANE Select NP_597677.2:n.8050-169G=
NM_015384.5:c.*335G= (NIPBL) NP_056199.2:n.*335G=