Canonical Allele Identifier: CA1539582554
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36985786A= , CM000667.2:g.36985786A= GRCh38
NC_000005.9:g.36985888A= , CM000667.1:g.36985888A= GRCh37
NC_000005.8:g.37021645A= NCBI36
NG_006987.1:g.113904A=
NG_006987.2:g.113904A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.2606A= MANE Select ENSP00000282516.8:p.Lys869=
ENST00000652901.1:c.2606A= ENSP00000499536.1:p.Lys869=
ENST00000282516.12:c.2606A= ENSP00000282516.8:p.Lys869=
ENST00000448238.2:c.2606A= ENSP00000406266.2:p.Lys869=
ENST00000504430.5:n.2226A=
ENST00000621733.1:c.1-78792A= ENSP00000480694.1:n.1-78792A=
NM_015384.4:c.2606A= NP_056199.2:p.Lys869=
NM_133433.3:c.2606A= NP_597677.2:p.Lys869=
XM_005248280.2:c.2606A= XP_005248337.1:p.Lys869=
XM_005248282.3:c.1862A= XP_005248339.2:p.Lys621=
XM_006714467.2:c.2606A= XP_006714530.1:p.Lys869=
XM_006714468.1:c.2606A= XP_006714531.1:p.Lys869=
XM_011514014.1:c.2606A= XP_011512316.1:p.Lys869=
XM_011514015.1:c.2606A= XP_011512317.1:p.Lys869=
XM_005248280.3:c.2606A= XP_005248337.1:p.Lys869=
XM_005248282.5:c.1946A= XP_005248339.3:p.Lys649=
XM_006714468.2:c.2606A= XP_006714531.1:p.Lys869=
XM_017009329.1:c.2606A= XP_016864818.1:p.Lys869=
XM_017009330.2:c.989A= XP_016864819.1:p.Lys330=
XM_017009331.1:c.1495+9384A= XP_016864820.1:n.1495+9384A=
NM_133433.4:c.2606A= MANE Select NP_597677.2:p.Lys869=
NM_015384.5:c.2606A= NP_056199.2:p.Lys869=