Canonical Allele Identifier: CA1539609262
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37010094A= , CM000667.2:g.37010094A= GRCh38
NC_000005.9:g.37010196A= , CM000667.1:g.37010196A= GRCh37
NC_000005.8:g.37045953A= NCBI36
NG_006987.1:g.138212A=
NG_006987.2:g.138212A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.4429A= MANE Select ENSP00000282516.8:p.Ser1477=
ENST00000652901.1:c.4429A= ENSP00000499536.1:p.Ser1477=
ENST00000282516.12:c.4429A= ENSP00000282516.8:p.Ser1477=
ENST00000448238.2:c.4429A= ENSP00000406266.2:p.Ser1477=
ENST00000621733.1:c.1-54484A= ENSP00000480694.1:n.1-54484A=
NM_015384.4:c.4429A= NP_056199.2:p.Ser1477=
NM_133433.3:c.4429A= NP_597677.2:p.Ser1477=
XM_005248280.2:c.4429A= XP_005248337.1:p.Ser1477=
XM_005248282.3:c.3685A= XP_005248339.2:p.Ser1229=
XM_006714467.2:c.4429A= XP_006714530.1:p.Ser1477=
XM_006714468.1:c.4231A= XP_006714531.1:p.Ser1411=
XM_011514014.1:c.4048A= XP_011512316.1:p.Ser1350=
XM_011514015.1:c.4429A= XP_011512317.1:p.Ser1477=
XM_005248280.3:c.4429A= XP_005248337.1:p.Ser1477=
XM_005248282.5:c.3769A= XP_005248339.3:p.Ser1257=
XM_006714468.2:c.4231A= XP_006714531.1:p.Ser1411=
XM_017009329.1:c.4429A= XP_016864818.1:p.Ser1477=
XM_017009330.2:c.2812A= XP_016864819.1:p.Ser938=
XM_017009331.1:c.2803A= XP_016864820.1:p.Ser935=
NM_133433.4:c.4429A= MANE Select NP_597677.2:p.Ser1477=
NM_015384.5:c.4429A= NP_056199.2:p.Ser1477=