Canonical Allele Identifier: CA1539588616
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37063828_37063866delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG , CM000667.2:g.37063828_37063866delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG GRCh38
NC_000005.9:g.37063930_37063968delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG , CM000667.1:g.37063930_37063968delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG GRCh37
NC_000005.8:g.37099687_37099725delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG NCBI36
NG_006987.1:g.191946_191984delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG
NG_006987.2:g.191946_191984delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG MANE Select ENSP00000282516.8:p.Glu2633=
ENST00000652901.1:c.7752_7790delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG ENSP00000499536.1:p.Glu2584=
ENST00000282516.12:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG ENSP00000282516.8:p.Glu2633=
ENST00000448238.2:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG ENSP00000406266.2:p.Glu2633=
ENST00000513819.1:c.302_340delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG ENSP00000421504.1:p.Lys101=
ENST00000514335.1:n.1781_1819delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG
ENST00000621733.1:c.1-750_1-712delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG ENSP00000480694.1:n.1-750_1-712delinsAGAAGAAGAAGGGGAGGTTTCAGC...
NM_015384.4:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG NP_056199.2:p.Glu2633=
NM_133433.3:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG NP_597677.2:p.Glu2633=
XM_005248280.2:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_005248337.1:p.Glu2633=
XM_005248282.3:c.7155_7193delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_005248339.2:p.Glu2385=
XM_006714467.2:c.7752_7790delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_006714530.1:p.Glu2584=
XM_006714468.1:c.7701_7739delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_006714531.1:p.Glu2567=
XM_011514014.1:c.7518_7556delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_011512316.1:p.Glu2506=
XM_005248280.3:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_005248337.1:p.Glu2633=
XM_005248282.5:c.7239_7277delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_005248339.3:p.Glu2413=
XM_006714468.2:c.7701_7739delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_006714531.1:p.Glu2567=
XM_017009329.1:c.7752_7790delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_016864818.1:p.Glu2584=
XM_017009330.2:c.6282_6320delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_016864819.1:p.Glu2094=
XM_017009331.1:c.6273_6311delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG XP_016864820.1:p.Glu2091=
NM_133433.4:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG MANE Select NP_597677.2:p.Glu2633=
NM_015384.5:c.7899_7937delinsAGAAGAAGAAGGGGAGGTTTCAGCTAGCACAAATGCTCG NP_056199.2:p.Glu2633=