Canonical Allele Identifier: CA1539582832
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36985923A= , CM000667.2:g.36985923A= GRCh38
NC_000005.9:g.36986025A= , CM000667.1:g.36986025A= GRCh37
NC_000005.8:g.37021782A= NCBI36
NG_006987.1:g.114041A=
NG_006987.2:g.114041A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.2743A= MANE Select ENSP00000282516.8:p.Ser915=
ENST00000652901.1:c.2743A= ENSP00000499536.1:p.Ser915=
ENST00000282516.12:c.2743A= ENSP00000282516.8:p.Ser915=
ENST00000448238.2:c.2743A= ENSP00000406266.2:p.Ser915=
ENST00000504430.5:n.2363A=
ENST00000621733.1:c.1-78655A= ENSP00000480694.1:n.1-78655A=
NM_015384.4:c.2743A= NP_056199.2:p.Ser915=
NM_133433.3:c.2743A= NP_597677.2:p.Ser915=
XM_005248280.2:c.2743A= XP_005248337.1:p.Ser915=
XM_005248282.3:c.1999A= XP_005248339.2:p.Ser667=
XM_006714467.2:c.2743A= XP_006714530.1:p.Ser915=
XM_006714468.1:c.2743A= XP_006714531.1:p.Ser915=
XM_011514014.1:c.2743A= XP_011512316.1:p.Ser915=
XM_011514015.1:c.2743A= XP_011512317.1:p.Ser915=
XM_005248280.3:c.2743A= XP_005248337.1:p.Ser915=
XM_005248282.5:c.2083A= XP_005248339.3:p.Ser695=
XM_006714468.2:c.2743A= XP_006714531.1:p.Ser915=
XM_017009329.1:c.2743A= XP_016864818.1:p.Ser915=
XM_017009330.2:c.1126A= XP_016864819.1:p.Ser376=
XM_017009331.1:c.1495+9521A= XP_016864820.1:n.1495+9521A=
NM_133433.4:c.2743A= MANE Select NP_597677.2:p.Ser915=
NM_015384.5:c.2743A= NP_056199.2:p.Ser915=