Canonical Allele Identifier: CA3237345
Gene: NIPBL HGNC NCBI
CPLANE1 HGNC NCBI

Linked Data

dbSNP Id: rs749178582
gnomAD v2: 5-37064797-A-C
gnomAD v4: 5-37064695-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37064695A>C , CM000667.2:g.37064695A>C GRCh38
NC_000005.9:g.37064797A>C , CM000667.1:g.37064797A>C GRCh37
NC_000005.8:g.37100554A>C NCBI36
NG_006987.1:g.192813A>C
NG_006987.2:g.192813A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.8218A>C (NIPBL) MANE Select ENSP00000282516.8:p.Met2740Leu
ENST00000652901.1:c.*162A>C (NIPBL) ENSP00000499536.1:n.*162A>C
ENST00000282516.12:c.8218A>C (NIPBL) ENSP00000282516.8:p.Met2740Leu
ENST00000514335.1:n.2141A>C (NIPBL)
ENST00000621733.1:c.118A>C (NIPBL) ENSP00000480694.1:p.Met40Leu
NM_015384.4:c.*672A>C (NIPBL) NP_056199.2:n.*672A>C
NM_133433.3:c.8218A>C (NIPBL) NP_597677.2:p.Met2740Leu
XM_005248280.2:c.*162A>C (NIPBL) XP_005248337.1:n.*162A>C
XM_005248282.3:c.7474A>C (NIPBL) XP_005248339.2:p.Met2492Leu
XM_006714467.2:c.8071A>C (NIPBL) XP_006714530.1:p.Met2691Leu
XM_006714468.1:c.8020A>C (NIPBL) XP_006714531.1:p.Met2674Leu
XM_011514014.1:c.7837A>C (NIPBL) XP_011512316.1:p.Met2613Leu
XM_005248280.3:c.*162A>C (NIPBL) XP_005248337.1:n.*162A>C
XM_005248282.5:c.7558A>C (NIPBL) XP_005248339.3:p.Met2520Leu
XM_006714468.2:c.8020A>C (NIPBL) XP_006714531.1:p.Met2674Leu
XM_017009329.1:c.*162A>C (NIPBL) XP_016864818.1:n.*162A>C
XM_017009330.2:c.6601A>C (NIPBL) XP_016864819.1:p.Met2201Leu
XM_017009331.1:c.6592A>C (NIPBL) XP_016864820.1:p.Met2198Leu
XR_925644.2:n.11987T>G (CPLANE1)
NM_133433.4:c.8218A>C (NIPBL) MANE Select NP_597677.2:p.Met2740Leu
NM_015384.5:c.*672A>C (NIPBL) NP_056199.2:n.*672A>C