Canonical Allele Identifier: CA359522797
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064738G>T , CM000667.2:g.37064738G>T GRCh38
NC_000005.9:g.37064840G>T , CM000667.1:g.37064840G>T GRCh37
NC_000005.8:g.37100597G>T NCBI36
NG_006987.1:g.192856G>T
NG_006987.2:g.192856G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8261G>T (NIPBL) MANE Select ENSP00000282516.8:p.Arg2754Leu
ENST00000652901.1:c.*205G>T (NIPBL) ENSP00000499536.1:n.*205G>T
ENST00000282516.12:c.8261G>T (NIPBL) ENSP00000282516.8:p.Arg2754Leu
ENST00000514335.1:n.2184G>T (NIPBL)
ENST00000621733.1:c.161G>T (NIPBL) ENSP00000480694.1:p.Arg54Leu
NM_015384.4:c.*715G>T (NIPBL) NP_056199.2:n.*715G>T
NM_133433.3:c.8261G>T (NIPBL) NP_597677.2:p.Arg2754Leu
XM_005248280.2:c.*205G>T (NIPBL) XP_005248337.1:n.*205G>T
XM_005248282.3:c.7517G>T (NIPBL) XP_005248339.2:p.Arg2506Leu
XM_006714467.2:c.8114G>T (NIPBL) XP_006714530.1:p.Arg2705Leu
XM_006714468.1:c.8063G>T (NIPBL) XP_006714531.1:p.Arg2688Leu
XM_011514014.1:c.7880G>T (NIPBL) XP_011512316.1:p.Arg2627Leu
XM_005248280.3:c.*205G>T (NIPBL) XP_005248337.1:n.*205G>T
XM_005248282.5:c.7601G>T (NIPBL) XP_005248339.3:p.Arg2534Leu
XM_006714468.2:c.8063G>T (NIPBL) XP_006714531.1:p.Arg2688Leu
XM_017009329.1:c.*205G>T (NIPBL) XP_016864818.1:n.*205G>T
XM_017009330.2:c.6644G>T (NIPBL) XP_016864819.1:p.Arg2215Leu
XM_017009331.1:c.6635G>T (NIPBL) XP_016864820.1:p.Arg2212Leu
XR_925644.2:n.11944C>A (CPLANE1)
NM_133433.4:c.8261G>T (NIPBL) MANE Select NP_597677.2:p.Arg2754Leu
NM_015384.5:c.*715G>T (NIPBL) NP_056199.2:n.*715G>T