Canonical Allele Identifier: CA1539583136
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37060988G= , CM000667.2:g.37060988G= GRCh38
NC_000005.9:g.37061090G= , CM000667.1:g.37061090G= GRCh37
NC_000005.8:g.37096847G= NCBI36
NG_006987.1:g.189106G=
NG_006987.2:g.189106G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.7830G= MANE Select ENSP00000282516.8:p.Val2610=
ENST00000652901.1:c.7683G= ENSP00000499536.1:p.Val2561=
ENST00000282516.12:c.7830G= ENSP00000282516.8:p.Val2610=
ENST00000448238.2:c.7830G= ENSP00000406266.2:p.Val2610=
ENST00000513819.1:c.263+1823G= ENSP00000421504.1:n.263+1823G=
ENST00000514335.1:n.1712G=
ENST00000621733.1:c.1-3590G= ENSP00000480694.1:n.1-3590G=
NM_015384.4:c.7830G= NP_056199.2:p.Val2610=
NM_133433.3:c.7830G= NP_597677.2:p.Val2610=
XM_005248280.2:c.7830G= XP_005248337.1:p.Val2610=
XM_005248282.3:c.7086G= XP_005248339.2:p.Val2362=
XM_006714467.2:c.7683G= XP_006714530.1:p.Val2561=
XM_006714468.1:c.7632G= XP_006714531.1:p.Val2544=
XM_011514014.1:c.7449G= XP_011512316.1:p.Val2483=
XM_005248280.3:c.7830G= XP_005248337.1:p.Val2610=
XM_005248282.5:c.7170G= XP_005248339.3:p.Val2390=
XM_006714468.2:c.7632G= XP_006714531.1:p.Val2544=
XM_017009329.1:c.7683G= XP_016864818.1:p.Val2561=
XM_017009330.2:c.6213G= XP_016864819.1:p.Val2071=
XM_017009331.1:c.6204G= XP_016864820.1:p.Val2068=
NM_133433.4:c.7830G= MANE Select NP_597677.2:p.Val2610=
NM_015384.5:c.7830G= NP_056199.2:p.Val2610=