Canonical Allele Identifier: CA359522256
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064614A>T , CM000667.2:g.37064614A>T GRCh38
NC_000005.9:g.37064716A>T , CM000667.1:g.37064716A>T GRCh37
NC_000005.8:g.37100473A>T NCBI36
NG_006987.1:g.192732A>T
NG_006987.2:g.192732A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8137A>T (NIPBL) MANE Select ENSP00000282516.8:p.Ile2713Phe
ENST00000652901.1:c.*81A>T (NIPBL) ENSP00000499536.1:n.*81A>T
ENST00000282516.12:c.8137A>T (NIPBL) ENSP00000282516.8:p.Ile2713Phe
ENST00000514335.1:n.2060A>T (NIPBL)
ENST00000621733.1:c.37A>T (NIPBL) ENSP00000480694.1:p.Ile13Phe
NM_015384.4:c.*591A>T (NIPBL) NP_056199.2:n.*591A>T
NM_133433.3:c.8137A>T (NIPBL) NP_597677.2:p.Ile2713Phe
XM_005248280.2:c.*81A>T (NIPBL) XP_005248337.1:n.*81A>T
XM_005248282.3:c.7393A>T (NIPBL) XP_005248339.2:p.Ile2465Phe
XM_006714467.2:c.7990A>T (NIPBL) XP_006714530.1:p.Ile2664Phe
XM_006714468.1:c.7939A>T (NIPBL) XP_006714531.1:p.Ile2647Phe
XM_011514014.1:c.7756A>T (NIPBL) XP_011512316.1:p.Ile2586Phe
XM_005248280.3:c.*81A>T (NIPBL) XP_005248337.1:n.*81A>T
XM_005248282.5:c.7477A>T (NIPBL) XP_005248339.3:p.Ile2493Phe
XM_006714468.2:c.7939A>T (NIPBL) XP_006714531.1:p.Ile2647Phe
XM_017009329.1:c.*81A>T (NIPBL) XP_016864818.1:n.*81A>T
XM_017009330.2:c.6520A>T (NIPBL) XP_016864819.1:p.Ile2174Phe
XM_017009331.1:c.6511A>T (NIPBL) XP_016864820.1:p.Ile2171Phe
XR_925644.2:n.12068T>A (CPLANE1)
NM_133433.4:c.8137A>T (NIPBL) MANE Select NP_597677.2:p.Ile2713Phe
NM_015384.5:c.*591A>T (NIPBL) NP_056199.2:n.*591A>T