Canonical Allele Identifier: CA359522381
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064644C>A , CM000667.2:g.37064644C>A GRCh38
NC_000005.9:g.37064746C>A , CM000667.1:g.37064746C>A GRCh37
NC_000005.8:g.37100503C>A NCBI36
NG_006987.1:g.192762C>A
NG_006987.2:g.192762C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8167C>A (NIPBL) MANE Select ENSP00000282516.8:p.Gln2723Lys
ENST00000652901.1:c.*111C>A (NIPBL) ENSP00000499536.1:n.*111C>A
ENST00000282516.12:c.8167C>A (NIPBL) ENSP00000282516.8:p.Gln2723Lys
ENST00000514335.1:n.2090C>A (NIPBL)
ENST00000621733.1:c.67C>A (NIPBL) ENSP00000480694.1:p.Gln23Lys
NM_015384.4:c.*621C>A (NIPBL) NP_056199.2:n.*621C>A
NM_133433.3:c.8167C>A (NIPBL) NP_597677.2:p.Gln2723Lys
XM_005248280.2:c.*111C>A (NIPBL) XP_005248337.1:n.*111C>A
XM_005248282.3:c.7423C>A (NIPBL) XP_005248339.2:p.Gln2475Lys
XM_006714467.2:c.8020C>A (NIPBL) XP_006714530.1:p.Gln2674Lys
XM_006714468.1:c.7969C>A (NIPBL) XP_006714531.1:p.Gln2657Lys
XM_011514014.1:c.7786C>A (NIPBL) XP_011512316.1:p.Gln2596Lys
XM_005248280.3:c.*111C>A (NIPBL) XP_005248337.1:n.*111C>A
XM_005248282.5:c.7507C>A (NIPBL) XP_005248339.3:p.Gln2503Lys
XM_006714468.2:c.7969C>A (NIPBL) XP_006714531.1:p.Gln2657Lys
XM_017009329.1:c.*111C>A (NIPBL) XP_016864818.1:n.*111C>A
XM_017009330.2:c.6550C>A (NIPBL) XP_016864819.1:p.Gln2184Lys
XM_017009331.1:c.6541C>A (NIPBL) XP_016864820.1:p.Gln2181Lys
XR_925644.2:n.12038G>T (CPLANE1)
NM_133433.4:c.8167C>A (NIPBL) MANE Select NP_597677.2:p.Gln2723Lys
NM_015384.5:c.*621C>A (NIPBL) NP_056199.2:n.*621C>A