Canonical Allele Identifier: CA359522232
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064608A>C , CM000667.2:g.37064608A>C GRCh38
NC_000005.9:g.37064710A>C , CM000667.1:g.37064710A>C GRCh37
NC_000005.8:g.37100467A>C NCBI36
NG_006987.1:g.192726A>C
NG_006987.2:g.192726A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8131A>C (NIPBL) MANE Select ENSP00000282516.8:p.Ile2711Leu
ENST00000652901.1:c.*75A>C (NIPBL) ENSP00000499536.1:n.*75A>C
ENST00000282516.12:c.8131A>C (NIPBL) ENSP00000282516.8:p.Ile2711Leu
ENST00000514335.1:n.2054A>C (NIPBL)
ENST00000621733.1:c.31A>C (NIPBL) ENSP00000480694.1:p.Ile11Leu
NM_015384.4:c.*585A>C (NIPBL) NP_056199.2:n.*585A>C
NM_133433.3:c.8131A>C (NIPBL) NP_597677.2:p.Ile2711Leu
XM_005248280.2:c.*75A>C (NIPBL) XP_005248337.1:n.*75A>C
XM_005248282.3:c.7387A>C (NIPBL) XP_005248339.2:p.Ile2463Leu
XM_006714467.2:c.7984A>C (NIPBL) XP_006714530.1:p.Ile2662Leu
XM_006714468.1:c.7933A>C (NIPBL) XP_006714531.1:p.Ile2645Leu
XM_011514014.1:c.7750A>C (NIPBL) XP_011512316.1:p.Ile2584Leu
XM_005248280.3:c.*75A>C (NIPBL) XP_005248337.1:n.*75A>C
XM_005248282.5:c.7471A>C (NIPBL) XP_005248339.3:p.Ile2491Leu
XM_006714468.2:c.7933A>C (NIPBL) XP_006714531.1:p.Ile2645Leu
XM_017009329.1:c.*75A>C (NIPBL) XP_016864818.1:n.*75A>C
XM_017009330.2:c.6514A>C (NIPBL) XP_016864819.1:p.Ile2172Leu
XM_017009331.1:c.6505A>C (NIPBL) XP_016864820.1:p.Ile2169Leu
XR_925644.2:n.12074T>G (CPLANE1)
NM_133433.4:c.8131A>C (NIPBL) MANE Select NP_597677.2:p.Ile2711Leu
NM_015384.5:c.*585A>C (NIPBL) NP_056199.2:n.*585A>C