Canonical Allele Identifier: CA1539582399
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36985693C= , CM000667.2:g.36985693C= GRCh38
NC_000005.9:g.36985795C= , CM000667.1:g.36985795C= GRCh37
NC_000005.8:g.37021552C= NCBI36
NG_006987.1:g.113811C=
NG_006987.2:g.113811C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.2513C= MANE Select ENSP00000282516.8:p.Ser838=
ENST00000652901.1:c.2513C= ENSP00000499536.1:p.Ser838=
ENST00000282516.12:c.2513C= ENSP00000282516.8:p.Ser838=
ENST00000448238.2:c.2513C= ENSP00000406266.2:p.Ser838=
ENST00000504430.5:n.2133C=
ENST00000621733.1:c.1-78885C= ENSP00000480694.1:n.1-78885C=
NM_015384.4:c.2513C= NP_056199.2:p.Ser838=
NM_133433.3:c.2513C= NP_597677.2:p.Ser838=
XM_005248280.2:c.2513C= XP_005248337.1:p.Ser838=
XM_005248282.3:c.1769C= XP_005248339.2:p.Ser590=
XM_006714467.2:c.2513C= XP_006714530.1:p.Ser838=
XM_006714468.1:c.2513C= XP_006714531.1:p.Ser838=
XM_011514014.1:c.2513C= XP_011512316.1:p.Ser838=
XM_011514015.1:c.2513C= XP_011512317.1:p.Ser838=
XM_005248280.3:c.2513C= XP_005248337.1:p.Ser838=
XM_005248282.5:c.1853C= XP_005248339.3:p.Ser618=
XM_006714468.2:c.2513C= XP_006714531.1:p.Ser838=
XM_017009329.1:c.2513C= XP_016864818.1:p.Ser838=
XM_017009330.2:c.896C= XP_016864819.1:p.Ser299=
XM_017009331.1:c.1495+9291C= XP_016864820.1:n.1495+9291C=
NM_133433.4:c.2513C= MANE Select NP_597677.2:p.Ser838=
NM_015384.5:c.2513C= NP_056199.2:p.Ser838=