Canonical Allele Identifier: CA1539592955
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36995786A= , CM000667.2:g.36995786A= GRCh38
NC_000005.9:g.36995888A= , CM000667.1:g.36995888A= GRCh37
NC_000005.8:g.37031645A= NCBI36
NG_006987.1:g.123904A=
NG_006987.2:g.123904A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.3286A= MANE Select ENSP00000282516.8:p.Ser1096=
ENST00000652901.1:c.3286A= ENSP00000499536.1:p.Ser1096=
ENST00000282516.12:c.3286A= ENSP00000282516.8:p.Ser1096=
ENST00000448238.2:c.3286A= ENSP00000406266.2:p.Ser1096=
ENST00000503274.1:n.637A=
ENST00000504430.5:n.2906A=
ENST00000509429.1:n.37A=
ENST00000621733.1:c.1-68792A= ENSP00000480694.1:n.1-68792A=
NM_015384.4:c.3286A= NP_056199.2:p.Ser1096=
NM_133433.3:c.3286A= NP_597677.2:p.Ser1096=
XM_005248280.2:c.3286A= XP_005248337.1:p.Ser1096=
XM_005248282.3:c.2542A= XP_005248339.2:p.Ser848=
XM_006714467.2:c.3286A= XP_006714530.1:p.Ser1096=
XM_006714468.1:c.3286A= XP_006714531.1:p.Ser1096=
XM_011514014.1:c.3122-5031A= XP_011512316.1:n.3122-5031A=
XM_011514015.1:c.3286A= XP_011512317.1:p.Ser1096=
XM_005248280.3:c.3286A= XP_005248337.1:p.Ser1096=
XM_005248282.5:c.2626A= XP_005248339.3:p.Ser876=
XM_006714468.2:c.3286A= XP_006714531.1:p.Ser1096=
XM_017009329.1:c.3286A= XP_016864818.1:p.Ser1096=
XM_017009330.2:c.1669A= XP_016864819.1:p.Ser557=
XM_017009331.1:c.1660A= XP_016864820.1:p.Ser554=
NM_133433.4:c.3286A= MANE Select NP_597677.2:p.Ser1096=
NM_015384.5:c.3286A= NP_056199.2:p.Ser1096=