Canonical Allele Identifier: CA1539590792
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064860C= , CM000667.2:g.37064860C= GRCh38
NC_000005.9:g.37064962C= , CM000667.1:g.37064962C= GRCh37
NC_000005.8:g.37100719C= NCBI36
NG_006987.1:g.192978C=
NG_006987.2:g.192978C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.8383C= (NIPBL) MANE Select ENSP00000282516.8:p.Leu2795=
ENST00000652901.1:c.*327C= (NIPBL) ENSP00000499536.1:n.*327C=
ENST00000282516.12:c.8383C= (NIPBL) ENSP00000282516.8:p.Leu2795=
ENST00000514335.1:n.2306C= (NIPBL)
ENST00000621733.1:c.283C= (NIPBL) ENSP00000480694.1:p.Leu95=
NM_015384.4:c.*837C= (NIPBL) NP_056199.2:n.*837C=
NM_133433.3:c.8383C= (NIPBL) NP_597677.2:p.Leu2795=
XM_005248280.2:c.*327C= (NIPBL) XP_005248337.1:n.*327C=
XM_005248282.3:c.7639C= (NIPBL) XP_005248339.2:p.Leu2547=
XM_006714467.2:c.8236C= (NIPBL) XP_006714530.1:p.Leu2746=
XM_006714468.1:c.8185C= (NIPBL) XP_006714531.1:p.Leu2729=
XM_011514014.1:c.8002C= (NIPBL) XP_011512316.1:p.Leu2668=
XM_005248280.3:c.*327C= (NIPBL) XP_005248337.1:n.*327C=
XM_005248282.5:c.7723C= (NIPBL) XP_005248339.3:p.Leu2575=
XM_006714468.2:c.8185C= (NIPBL) XP_006714531.1:p.Leu2729=
XM_017009329.1:c.*327C= (NIPBL) XP_016864818.1:n.*327C=
XM_017009330.2:c.6766C= (NIPBL) XP_016864819.1:p.Leu2256=
XM_017009331.1:c.6757C= (NIPBL) XP_016864820.1:p.Leu2253=
XR_925644.2:n.11822G= (CPLANE1)
NM_133433.4:c.8383C= (NIPBL) MANE Select NP_597677.2:p.Leu2795=
NM_015384.5:c.*837C= (NIPBL) NP_056199.2:n.*837C=