Canonical Allele Identifier: CA1539578148
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36958123G= , CM000667.2:g.36958123G= GRCh38
NC_000005.9:g.36958225G= , CM000667.1:g.36958225G= GRCh37
NC_000005.8:g.36993982G= NCBI36
NG_006987.1:g.86241G=
NG_006987.2:g.86241G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.250G= MANE Select ENSP00000282516.8:p.Gly84=
ENST00000652901.1:c.250G= ENSP00000499536.1:p.Gly84=
ENST00000282516.12:c.250G= ENSP00000282516.8:p.Gly84=
ENST00000448238.2:c.250G= ENSP00000406266.2:p.Gly84=
ENST00000505998.5:n.229G=
ENST00000621733.1:c.-1+81101G= ENSP00000480694.1:n.-1+81101G=
NM_015384.4:c.250G= NP_056199.2:p.Gly84=
NM_133433.3:c.250G= NP_597677.2:p.Gly84=
XM_005248280.2:c.250G= XP_005248337.1:p.Gly84=
XM_006714467.2:c.250G= XP_006714530.1:p.Gly84=
XM_006714468.1:c.250G= XP_006714531.1:p.Gly84=
XM_011514014.1:c.250G= XP_011512316.1:p.Gly84=
XM_011514015.1:c.250G= XP_011512317.1:p.Gly84=
XM_005248280.3:c.250G= XP_005248337.1:p.Gly84=
XM_006714468.2:c.250G= XP_006714531.1:p.Gly84=
XM_017009329.1:c.250G= XP_016864818.1:p.Gly84=
XM_017009331.1:c.250G= XP_016864820.1:p.Gly84=
NM_133433.4:c.250G= MANE Select NP_597677.2:p.Gly84=
NM_015384.5:c.250G= NP_056199.2:p.Gly84=