Canonical Allele Identifier: CA359523700
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064854C>G , CM000667.2:g.37064854C>G GRCh38
NC_000005.9:g.37064956C>G , CM000667.1:g.37064956C>G GRCh37
NC_000005.8:g.37100713C>G NCBI36
NG_006987.1:g.192972C>G
NG_006987.2:g.192972C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.8377C>G (NIPBL) MANE Select ENSP00000282516.8:p.Arg2793Gly
ENST00000652901.1:c.*321C>G (NIPBL) ENSP00000499536.1:n.*321C>G
ENST00000282516.12:c.8377C>G (NIPBL) ENSP00000282516.8:p.Arg2793Gly
ENST00000514335.1:n.2300C>G (NIPBL)
ENST00000621733.1:c.277C>G (NIPBL) ENSP00000480694.1:p.Arg93Gly
NM_015384.4:c.*831C>G (NIPBL) NP_056199.2:n.*831C>G
NM_133433.3:c.8377C>G (NIPBL) NP_597677.2:p.Arg2793Gly
XM_005248280.2:c.*321C>G (NIPBL) XP_005248337.1:n.*321C>G
XM_005248282.3:c.7633C>G (NIPBL) XP_005248339.2:p.Arg2545Gly
XM_006714467.2:c.8230C>G (NIPBL) XP_006714530.1:p.Arg2744Gly
XM_006714468.1:c.8179C>G (NIPBL) XP_006714531.1:p.Arg2727Gly
XM_011514014.1:c.7996C>G (NIPBL) XP_011512316.1:p.Arg2666Gly
XM_005248280.3:c.*321C>G (NIPBL) XP_005248337.1:n.*321C>G
XM_005248282.5:c.7717C>G (NIPBL) XP_005248339.3:p.Arg2573Gly
XM_006714468.2:c.8179C>G (NIPBL) XP_006714531.1:p.Arg2727Gly
XM_017009329.1:c.*321C>G (NIPBL) XP_016864818.1:n.*321C>G
XM_017009330.2:c.6760C>G (NIPBL) XP_016864819.1:p.Arg2254Gly
XM_017009331.1:c.6751C>G (NIPBL) XP_016864820.1:p.Arg2251Gly
XR_925644.2:n.11828G>C (CPLANE1)
NM_133433.4:c.8377C>G (NIPBL) MANE Select NP_597677.2:p.Arg2793Gly
NM_015384.5:c.*831C>G (NIPBL) NP_056199.2:n.*831C>G