Canonical Allele Identifier: CA359519102
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37060983G>A , CM000667.2:g.37060983G>A GRCh38
NC_000005.9:g.37061085G>A , CM000667.1:g.37061085G>A GRCh37
NC_000005.8:g.37096842G>A NCBI36
NG_006987.1:g.189101G>A
NG_006987.2:g.189101G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.7825G>A MANE Select ENSP00000282516.8:p.Glu2609Lys
ENST00000652901.1:c.7678G>A ENSP00000499536.1:p.Glu2560Lys
ENST00000282516.12:c.7825G>A ENSP00000282516.8:p.Glu2609Lys
ENST00000448238.2:c.7825G>A ENSP00000406266.2:p.Glu2609Lys
ENST00000513819.1:c.263+1818G>A ENSP00000421504.1:n.263+1818G>A
ENST00000514335.1:n.1707G>A
ENST00000621733.1:c.1-3595G>A ENSP00000480694.1:n.1-3595G>A
NM_015384.4:c.7825G>A NP_056199.2:p.Glu2609Lys
NM_133433.3:c.7825G>A NP_597677.2:p.Glu2609Lys
XM_005248280.2:c.7825G>A XP_005248337.1:p.Glu2609Lys
XM_005248282.3:c.7081G>A XP_005248339.2:p.Glu2361Lys
XM_006714467.2:c.7678G>A XP_006714530.1:p.Glu2560Lys
XM_006714468.1:c.7627G>A XP_006714531.1:p.Glu2543Lys
XM_011514014.1:c.7444G>A XP_011512316.1:p.Glu2482Lys
XM_005248280.3:c.7825G>A XP_005248337.1:p.Glu2609Lys
XM_005248282.5:c.7165G>A XP_005248339.3:p.Glu2389Lys
XM_006714468.2:c.7627G>A XP_006714531.1:p.Glu2543Lys
XM_017009329.1:c.7678G>A XP_016864818.1:p.Glu2560Lys
XM_017009330.2:c.6208G>A XP_016864819.1:p.Glu2070Lys
XM_017009331.1:c.6199G>A XP_016864820.1:p.Glu2067Lys
NM_133433.4:c.7825G>A MANE Select NP_597677.2:p.Glu2609Lys
NM_015384.5:c.7825G>A NP_056199.2:p.Glu2609Lys