Canonical Allele Identifier: CA1539567602
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37048569T= , CM000667.2:g.37048569T= GRCh38
NC_000005.9:g.37048671T= , CM000667.1:g.37048671T= GRCh37
NC_000005.8:g.37084428T= NCBI36
NG_006987.1:g.176687T=
NG_006987.2:g.176687T=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.6657T= MANE Select ENSP00000282516.8:p.Ile2219=
ENST00000652901.1:c.6657T= ENSP00000499536.1:p.Ile2219=
ENST00000282516.12:c.6657T= ENSP00000282516.8:p.Ile2219=
ENST00000448238.2:c.6657T= ENSP00000406266.2:p.Ile2219=
ENST00000621733.1:c.1-16009T= ENSP00000480694.1:n.1-16009T=
NM_015384.4:c.6657T= NP_056199.2:p.Ile2219=
NM_133433.3:c.6657T= NP_597677.2:p.Ile2219=
XM_005248280.2:c.6657T= XP_005248337.1:p.Ile2219=
XM_005248282.3:c.5913T= XP_005248339.2:p.Ile1971=
XM_006714467.2:c.6657T= XP_006714530.1:p.Ile2219=
XM_006714468.1:c.6459T= XP_006714531.1:p.Ile2153=
XM_011514014.1:c.6276T= XP_011512316.1:p.Ile2092=
XM_011514015.1:c.6657T= XP_011512317.1:p.Ile2219=
XM_005248280.3:c.6657T= XP_005248337.1:p.Ile2219=
XM_005248282.5:c.5997T= XP_005248339.3:p.Ile1999=
XM_006714468.2:c.6459T= XP_006714531.1:p.Ile2153=
XM_017009329.1:c.6657T= XP_016864818.1:p.Ile2219=
XM_017009330.2:c.5040T= XP_016864819.1:p.Ile1680=
XM_017009331.1:c.5031T= XP_016864820.1:p.Ile1677=
NM_133433.4:c.6657T= MANE Select NP_597677.2:p.Ile2219=
NM_015384.5:c.6657T= NP_056199.2:p.Ile2219=