Canonical Allele Identifier: CA2695204349
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37020668del , CM000667.2:g.37020668del GRCh38
NC_000005.9:g.37020770del , CM000667.1:g.37020770del GRCh37
NC_000005.8:g.37056527del NCBI36
NG_006987.1:g.148786del
NG_006987.2:g.148786del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.5220del MANE Select ENSP00000282516.8:p.Leu1741Ter
ENST00000652901.1:c.5220del ENSP00000499536.1:p.Leu1741Ter
ENST00000282516.12:c.5220del ENSP00000282516.8:p.Leu1741Ter
ENST00000448238.2:c.5220del ENSP00000406266.2:p.Leu1741Ter
ENST00000621733.1:c.1-43910del ENSP00000480694.1:n.1-43910del
NM_015384.4:c.5220del NP_056199.2:p.Leu1741Ter
NM_133433.3:c.5220del NP_597677.2:p.Leu1741Ter
XM_005248280.2:c.5220del XP_005248337.1:p.Leu1741Ter
XM_005248282.3:c.4476del XP_005248339.2:p.Leu1493Ter
XM_006714467.2:c.5220del XP_006714530.1:p.Leu1741Ter
XM_006714468.1:c.5022del XP_006714531.1:p.Leu1675Ter
XM_011514014.1:c.4839del XP_011512316.1:p.Leu1614Ter
XM_011514015.1:c.5220del XP_011512317.1:p.Leu1741Ter
XM_005248280.3:c.5220del XP_005248337.1:p.Leu1741Ter
XM_005248282.5:c.4560del XP_005248339.3:p.Leu1521Ter
XM_006714468.2:c.5022del XP_006714531.1:p.Leu1675Ter
XM_017009329.1:c.5220del XP_016864818.1:p.Leu1741Ter
XM_017009330.2:c.3603del XP_016864819.1:p.Leu1202Ter
XM_017009331.1:c.3594del XP_016864820.1:p.Leu1199Ter
NM_133433.4:c.5220del MANE Select NP_597677.2:p.Leu1741Ter
NM_015384.5:c.5220del NP_056199.2:p.Leu1741Ter