Canonical Allele Identifier: CA1539611504
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37038681C= , CM000667.2:g.37038681C= GRCh38
NC_000005.9:g.37038783C= , CM000667.1:g.37038783C= GRCh37
NC_000005.8:g.37074540C= NCBI36
NG_006987.1:g.166799C=
NG_006987.2:g.166799C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.6051C= MANE Select ENSP00000282516.8:p.Pro2017=
ENST00000652901.1:c.6051C= ENSP00000499536.1:p.Pro2017=
ENST00000282516.12:c.6051C= ENSP00000282516.8:p.Pro2017=
ENST00000448238.2:c.6051C= ENSP00000406266.2:p.Pro2017=
ENST00000621733.1:c.1-25897C= ENSP00000480694.1:n.1-25897C=
NM_015384.4:c.6051C= NP_056199.2:p.Pro2017=
NM_133433.3:c.6051C= NP_597677.2:p.Pro2017=
XM_005248280.2:c.6051C= XP_005248337.1:p.Pro2017=
XM_005248282.3:c.5307C= XP_005248339.2:p.Pro1769=
XM_006714467.2:c.6051C= XP_006714530.1:p.Pro2017=
XM_006714468.1:c.5853C= XP_006714531.1:p.Pro1951=
XM_011514014.1:c.5670C= XP_011512316.1:p.Pro1890=
XM_011514015.1:c.6051C= XP_011512317.1:p.Pro2017=
XM_005248280.3:c.6051C= XP_005248337.1:p.Pro2017=
XM_005248282.5:c.5391C= XP_005248339.3:p.Pro1797=
XM_006714468.2:c.5853C= XP_006714531.1:p.Pro1951=
XM_017009329.1:c.6051C= XP_016864818.1:p.Pro2017=
XM_017009330.2:c.4434C= XP_016864819.1:p.Pro1478=
XM_017009331.1:c.4425C= XP_016864820.1:p.Pro1475=
NM_133433.4:c.6051C= MANE Select NP_597677.2:p.Pro2017=
NM_015384.5:c.6051C= NP_056199.2:p.Pro2017=