Canonical Allele Identifier: CA559295087
Gene: NIPBL HGNC NCBI

Linked Data

dbSNP Id: rs1272105879

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36995511dup , CM000667.2:g.36995511dup GRCh38
NC_000005.9:g.36995613dup , CM000667.1:g.36995613dup GRCh37
NC_000005.8:g.37031370dup NCBI36
NG_006987.1:g.123629dup
NG_006987.2:g.123629dup

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.3122-111dup MANE Select ENSP00000282516.8:n.3122-111dup
ENST00000652901.1:c.3122-111dup ENSP00000499536.1:n.3122-111dup
ENST00000282516.12:c.3122-111dup ENSP00000282516.8:n.3122-111dup
ENST00000448238.2:c.3122-111dup ENSP00000406266.2:n.3122-111dup
ENST00000503274.1:n.362dup
ENST00000504430.5:n.2742-111dup
ENST00000621733.1:c.1-69067dup ENSP00000480694.1:n.1-69067dup
NM_015384.4:c.3122-111dup NP_056199.2:n.3122-111dup
NM_133433.3:c.3122-111dup NP_597677.2:n.3122-111dup
XM_005248280.2:c.3122-111dup XP_005248337.1:n.3122-111dup
XM_005248282.3:c.2378-111dup XP_005248339.2:n.2378-111dup
XM_006714467.2:c.3122-111dup XP_006714530.1:n.3122-111dup
XM_006714468.1:c.3122-111dup XP_006714531.1:n.3122-111dup
XM_011514014.1:c.3122-5306dup XP_011512316.1:n.3122-5306dup
XM_011514015.1:c.3122-111dup XP_011512317.1:n.3122-111dup
XM_005248280.3:c.3122-111dup XP_005248337.1:n.3122-111dup
XM_005248282.5:c.2462-111dup XP_005248339.3:n.2462-111dup
XM_006714468.2:c.3122-111dup XP_006714531.1:n.3122-111dup
XM_017009329.1:c.3122-111dup XP_016864818.1:n.3122-111dup
XM_017009330.2:c.1505-111dup XP_016864819.1:n.1505-111dup
XM_017009331.1:c.1496-111dup XP_016864820.1:n.1496-111dup
NM_133433.4:c.3122-111dup MANE Select NP_597677.2:n.3122-111dup
NM_015384.5:c.3122-111dup NP_056199.2:n.3122-111dup