Canonical Allele Identifier: CA1539573880
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36955610G= , CM000667.2:g.36955610G= GRCh38
NC_000005.9:g.36955712G= , CM000667.1:g.36955712G= GRCh37
NC_000005.8:g.36991469G= NCBI36
NG_006987.1:g.83728G=
NG_006987.2:g.83728G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.203G= MANE Select ENSP00000282516.8:p.Ser68=
ENST00000652901.1:c.203G= ENSP00000499536.1:p.Ser68=
ENST00000282516.12:c.203G= ENSP00000282516.8:p.Ser68=
ENST00000448238.2:c.203G= ENSP00000406266.2:p.Ser68=
ENST00000505998.5:n.182G=
ENST00000621733.1:c.-1+78588G= ENSP00000480694.1:n.-1+78588G=
NM_015384.4:c.203G= NP_056199.2:p.Ser68=
NM_133433.3:c.203G= NP_597677.2:p.Ser68=
XM_005248280.2:c.203G= XP_005248337.1:p.Ser68=
XM_006714467.2:c.203G= XP_006714530.1:p.Ser68=
XM_006714468.1:c.203G= XP_006714531.1:p.Ser68=
XM_011514014.1:c.203G= XP_011512316.1:p.Ser68=
XM_011514015.1:c.203G= XP_011512317.1:p.Ser68=
XM_005248280.3:c.203G= XP_005248337.1:p.Ser68=
XM_006714468.2:c.203G= XP_006714531.1:p.Ser68=
XM_017009329.1:c.203G= XP_016864818.1:p.Ser68=
XM_017009331.1:c.203G= XP_016864820.1:p.Ser68=
NM_133433.4:c.203G= MANE Select NP_597677.2:p.Ser68=
NM_015384.5:c.203G= NP_056199.2:p.Ser68=