Canonical Allele Identifier: CA359488118
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36976396G>T , CM000667.2:g.36976396G>T GRCh38
NC_000005.9:g.36976498G>T , CM000667.1:g.36976498G>T GRCh37
NC_000005.8:g.37012255G>T NCBI36
NG_006987.1:g.104514G>T
NG_006987.2:g.104514G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.1489G>T MANE Select ENSP00000282516.8:p.Asp497Tyr
ENST00000652901.1:c.1489G>T ENSP00000499536.1:p.Asp497Tyr
ENST00000282516.12:c.1489G>T ENSP00000282516.8:p.Asp497Tyr
ENST00000448238.2:c.1489G>T ENSP00000406266.2:p.Asp497Tyr
ENST00000504430.5:n.1109G>T
ENST00000621733.1:c.1-88182G>T ENSP00000480694.1:p.=
NM_015384.4:c.1489G>T NP_056199.2:p.Asp497Tyr
NM_133433.3:c.1489G>T NP_597677.2:p.Asp497Tyr
XM_005248280.2:c.1489G>T XP_005248337.1:p.Asp497Tyr
XM_005248282.3:c.745G>T XP_005248339.2:p.Asp249Tyr
XM_006714467.2:c.1489G>T XP_006714530.1:p.Asp497Tyr
XM_006714468.1:c.1489G>T XP_006714531.1:p.Asp497Tyr
XM_011514014.1:c.1489G>T XP_011512316.1:p.Asp497Tyr
XM_011514015.1:c.1489G>T XP_011512317.1:p.Asp497Tyr
XM_005248280.3:c.1489G>T XP_005248337.1:p.Asp497Tyr
XM_005248282.5:c.829G>T XP_005248339.3:p.Asp277Tyr
XM_006714468.2:c.1489G>T XP_006714531.1:p.Asp497Tyr
XM_017009329.1:c.1489G>T XP_016864818.1:p.Asp497Tyr
XM_017009331.1:c.1489G>T XP_016864820.1:p.Asp497Tyr
NM_133433.4:c.1489G>T MANE Select NP_597677.2:p.Asp497Tyr
NM_015384.5:c.1489G>T NP_056199.2:p.Asp497Tyr