Canonical Allele Identifier: CA1539618591
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37045577G= , CM000667.2:g.37045577G= GRCh38
NC_000005.9:g.37045679G= , CM000667.1:g.37045679G= GRCh37
NC_000005.8:g.37081436G= NCBI36
NG_006987.1:g.173695G=
NG_006987.2:g.173695G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.6478G= MANE Select ENSP00000282516.8:p.Asp2160=
ENST00000652901.1:c.6478G= ENSP00000499536.1:p.Asp2160=
ENST00000282516.12:c.6478G= ENSP00000282516.8:p.Asp2160=
ENST00000448238.2:c.6478G= ENSP00000406266.2:p.Asp2160=
ENST00000621733.1:c.1-19001G= ENSP00000480694.1:n.1-19001G=
NM_015384.4:c.6478G= NP_056199.2:p.Asp2160=
NM_133433.3:c.6478G= NP_597677.2:p.Asp2160=
XM_005248280.2:c.6478G= XP_005248337.1:p.Asp2160=
XM_005248282.3:c.5734G= XP_005248339.2:p.Asp1912=
XM_006714467.2:c.6478G= XP_006714530.1:p.Asp2160=
XM_006714468.1:c.6280G= XP_006714531.1:p.Asp2094=
XM_011514014.1:c.6097G= XP_011512316.1:p.Asp2033=
XM_011514015.1:c.6478G= XP_011512317.1:p.Asp2160=
XM_005248280.3:c.6478G= XP_005248337.1:p.Asp2160=
XM_005248282.5:c.5818G= XP_005248339.3:p.Asp1940=
XM_006714468.2:c.6280G= XP_006714531.1:p.Asp2094=
XM_017009329.1:c.6478G= XP_016864818.1:p.Asp2160=
XM_017009330.2:c.4861G= XP_016864819.1:p.Asp1621=
XM_017009331.1:c.4852G= XP_016864820.1:p.Asp1618=
NM_133433.4:c.6478G= MANE Select NP_597677.2:p.Asp2160=
NM_015384.5:c.6478G= NP_056199.2:p.Asp2160=