Canonical Allele Identifier: CA1075102131
Gene: NIPBL HGNC NCBI

Linked Data

dbSNP Id: rs1754580448

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37060776del , CM000667.2:g.37060776del GRCh38
NC_000005.9:g.37060878del , CM000667.1:g.37060878del GRCh37
NC_000005.8:g.37096635del NCBI36
NG_006987.1:g.188894del
NG_006987.2:g.188894del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.7686-68del MANE Select ENSP00000282516.8:n.7686-68del
ENST00000652901.1:c.7539-68del ENSP00000499536.1:n.7539-68del
ENST00000282516.12:c.7686-68del ENSP00000282516.8:n.7686-68del
ENST00000448238.2:c.7686-68del ENSP00000406266.2:n.7686-68del
ENST00000513819.1:c.263+1611del ENSP00000421504.1:n.263+1611del
ENST00000514335.1:n.1568-68del
ENST00000621733.1:c.1-3802del ENSP00000480694.1:n.1-3802del
NM_015384.4:c.7686-68del NP_056199.2:n.7686-68del
NM_133433.3:c.7686-68del NP_597677.2:n.7686-68del
XM_005248280.2:c.7686-68del XP_005248337.1:n.7686-68del
XM_005248282.3:c.6942-68del XP_005248339.2:n.6942-68del
XM_006714467.2:c.7539-68del XP_006714530.1:n.7539-68del
XM_006714468.1:c.7488-68del XP_006714531.1:n.7488-68del
XM_011514014.1:c.7305-68del XP_011512316.1:n.7305-68del
XM_011514015.1:c.7264-68del XP_011512317.1:n.7264-68del
XM_005248280.3:c.7686-68del XP_005248337.1:n.7686-68del
XM_005248282.5:c.7026-68del XP_005248339.3:n.7026-68del
XM_006714468.2:c.7488-68del XP_006714531.1:n.7488-68del
XM_017009329.1:c.7539-68del XP_016864818.1:n.7539-68del
XM_017009330.2:c.6069-68del XP_016864819.1:n.6069-68del
XM_017009331.1:c.6060-68del XP_016864820.1:n.6060-68del
NM_133433.4:c.7686-68del MANE Select NP_597677.2:n.7686-68del
NM_015384.5:c.7686-68del NP_056199.2:n.7686-68del