Canonical Allele Identifier: CA1539584052
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37020636A= , CM000667.2:g.37020636A= GRCh38
NC_000005.9:g.37020738A= , CM000667.1:g.37020738A= GRCh37
NC_000005.8:g.37056495A= NCBI36
NG_006987.1:g.148754A=
NG_006987.2:g.148754A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.5188A= MANE Select ENSP00000282516.8:p.Ile1730=
ENST00000652901.1:c.5188A= ENSP00000499536.1:p.Ile1730=
ENST00000282516.12:c.5188A= ENSP00000282516.8:p.Ile1730=
ENST00000448238.2:c.5188A= ENSP00000406266.2:p.Ile1730=
ENST00000621733.1:c.1-43942A= ENSP00000480694.1:n.1-43942A=
NM_015384.4:c.5188A= NP_056199.2:p.Ile1730=
NM_133433.3:c.5188A= NP_597677.2:p.Ile1730=
XM_005248280.2:c.5188A= XP_005248337.1:p.Ile1730=
XM_005248282.3:c.4444A= XP_005248339.2:p.Ile1482=
XM_006714467.2:c.5188A= XP_006714530.1:p.Ile1730=
XM_006714468.1:c.4990A= XP_006714531.1:p.Ile1664=
XM_011514014.1:c.4807A= XP_011512316.1:p.Ile1603=
XM_011514015.1:c.5188A= XP_011512317.1:p.Ile1730=
XM_005248280.3:c.5188A= XP_005248337.1:p.Ile1730=
XM_005248282.5:c.4528A= XP_005248339.3:p.Ile1510=
XM_006714468.2:c.4990A= XP_006714531.1:p.Ile1664=
XM_017009329.1:c.5188A= XP_016864818.1:p.Ile1730=
XM_017009330.2:c.3571A= XP_016864819.1:p.Ile1191=
XM_017009331.1:c.3562A= XP_016864820.1:p.Ile1188=
NM_133433.4:c.5188A= MANE Select NP_597677.2:p.Ile1730=
NM_015384.5:c.5188A= NP_056199.2:p.Ile1730=