Canonical Allele Identifier: CA359521753
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064532G>T , CM000667.2:g.37064532G>T GRCh38
NC_000005.9:g.37064634G>T , CM000667.1:g.37064634G>T GRCh37
NC_000005.8:g.37100391G>T NCBI36
NG_006987.1:g.192650G>T
NG_006987.2:g.192650G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8055G>T (NIPBL) MANE Select ENSP00000282516.8:p.Leu2685Phe
ENST00000652901.1:c.7949G>T (NIPBL) ENSP00000499536.1:p.Ter2650Leu
ENST00000282516.12:c.8055G>T (NIPBL) ENSP00000282516.8:p.Leu2685Phe
ENST00000514335.1:n.1978G>T (NIPBL)
ENST00000621733.1:c.1-46G>T (NIPBL) ENSP00000480694.1:n.1-46G>T
NM_015384.4:c.*509G>T (NIPBL) NP_056199.2:n.*509G>T
NM_133433.3:c.8055G>T (NIPBL) NP_597677.2:p.Leu2685Phe
XM_005248280.2:c.8096G>T (NIPBL) XP_005248337.1:p.Ter2699Leu
XM_005248282.3:c.7311G>T (NIPBL) XP_005248339.2:p.Leu2437Phe
XM_006714467.2:c.7908G>T (NIPBL) XP_006714530.1:p.Leu2636Phe
XM_006714468.1:c.7857G>T (NIPBL) XP_006714531.1:p.Leu2619Phe
XM_011514014.1:c.7674G>T (NIPBL) XP_011512316.1:p.Leu2558Phe
XM_005248280.3:c.8096G>T (NIPBL) XP_005248337.1:p.Ter2699Leu
XM_005248282.5:c.7395G>T (NIPBL) XP_005248339.3:p.Leu2465Phe
XM_006714468.2:c.7857G>T (NIPBL) XP_006714531.1:p.Leu2619Phe
XM_017009329.1:c.7949G>T (NIPBL) XP_016864818.1:p.Ter2650Leu
XM_017009330.2:c.6438G>T (NIPBL) XP_016864819.1:p.Leu2146Phe
XM_017009331.1:c.6429G>T (NIPBL) XP_016864820.1:p.Leu2143Phe
XR_925644.2:n.12150C>A (CPLANE1)
NM_133433.4:c.8055G>T (NIPBL) MANE Select NP_597677.2:p.Leu2685Phe
NM_015384.5:c.*509G>T (NIPBL) NP_056199.2:n.*509G>T