Canonical Allele Identifier: CA2739289744
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36985201del , CM000667.2:g.36985201del GRCh38
NC_000005.9:g.36985303del , CM000667.1:g.36985303del GRCh37
NC_000005.8:g.37021060del NCBI36
NG_006987.1:g.113319del
NG_006987.2:g.113319del

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.2021del MANE Select ENSP00000282516.8:p.Asn674MetfsTer?
ENST00000652901.1:c.2021del ENSP00000499536.1:p.Asn674MetfsTer?
ENST00000282516.12:c.2021del ENSP00000282516.8:p.Asn674MetfsTer?
ENST00000448238.2:c.2021del ENSP00000406266.2:p.Asn674MetfsTer?
ENST00000504430.5:n.1641del
ENST00000621733.1:c.1-79377del ENSP00000480694.1:n.1-79377del
NM_015384.4:c.2021del NP_056199.2:p.Asn674MetfsTer?
NM_133433.3:c.2021del NP_597677.2:p.Asn674MetfsTer?
XM_005248280.2:c.2021del XP_005248337.1:p.Asn674MetfsTer?
XM_005248282.3:c.1277del XP_005248339.2:p.Asn426MetfsTer?
XM_006714467.2:c.2021del XP_006714530.1:p.Asn674MetfsTer?
XM_006714468.1:c.2021del XP_006714531.1:p.Asn674MetfsTer?
XM_011514014.1:c.2021del XP_011512316.1:p.Asn674MetfsTer?
XM_011514015.1:c.2021del XP_011512317.1:p.Asn674MetfsTer?
XM_005248280.3:c.2021del XP_005248337.1:p.Asn674MetfsTer?
XM_005248282.5:c.1361del XP_005248339.3:p.Asn454MetfsTer?
XM_006714468.2:c.2021del XP_006714531.1:p.Asn674MetfsTer?
XM_017009329.1:c.2021del XP_016864818.1:p.Asn674MetfsTer?
XM_017009330.2:c.404del XP_016864819.1:p.Asn135MetfsTer?
XM_017009331.1:c.1495+8799del XP_016864820.1:n.1495+8799del
NM_133433.4:c.2021del MANE Select NP_597677.2:p.Asn674MetfsTer?
NM_015384.5:c.2021del NP_056199.2:p.Asn674MetfsTer?