Canonical Allele Identifier: CA1539568892
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36975798_36975799delinsAC , CM000667.2:g.36975798_36975799delinsAC GRCh38
NC_000005.9:g.36975900_36975901delinsAC , CM000667.1:g.36975900_36975901delinsAC GRCh37
NC_000005.8:g.37011657_37011658delinsAC NCBI36
NG_006987.1:g.103916_103917delinsAC
NG_006987.2:g.103916_103917delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.891_892delinsAC MANE Select ENSP00000282516.8:p.Leu297=
ENST00000652901.1:c.891_892delinsAC ENSP00000499536.1:p.Leu297=
ENST00000282516.12:c.891_892delinsAC ENSP00000282516.8:p.Leu297=
ENST00000448238.2:c.891_892delinsAC ENSP00000406266.2:p.Leu297=
ENST00000504430.5:n.511_512delinsAC
ENST00000505998.5:n.870_871delinsAC
ENST00000621733.1:c.1-88780_1-88779delinsAC ENSP00000480694.1:n.1-88780_1-88779delinsAC
NM_015384.4:c.891_892delinsAC NP_056199.2:p.Leu297=
NM_133433.3:c.891_892delinsAC NP_597677.2:p.Leu297=
XM_005248280.2:c.891_892delinsAC XP_005248337.1:p.Leu297=
XM_005248282.3:c.147_148delinsAC XP_005248339.2:p.Leu49=
XM_006714467.2:c.891_892delinsAC XP_006714530.1:p.Leu297=
XM_006714468.1:c.891_892delinsAC XP_006714531.1:p.Leu297=
XM_011514014.1:c.891_892delinsAC XP_011512316.1:p.Leu297=
XM_011514015.1:c.891_892delinsAC XP_011512317.1:p.Leu297=
XM_005248280.3:c.891_892delinsAC XP_005248337.1:p.Leu297=
XM_005248282.5:c.231_232delinsAC XP_005248339.3:p.Leu77=
XM_006714468.2:c.891_892delinsAC XP_006714531.1:p.Leu297=
XM_017009329.1:c.891_892delinsAC XP_016864818.1:p.Leu297=
XM_017009331.1:c.891_892delinsAC XP_016864820.1:p.Leu297=
NM_133433.4:c.891_892delinsAC MANE Select NP_597677.2:p.Leu297=
NM_015384.5:c.891_892delinsAC NP_056199.2:p.Leu297=