Canonical Allele Identifier: CA1539601988
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37001334_37001335delinsAC , CM000667.2:g.37001334_37001335delinsAC GRCh38
NC_000005.9:g.37001436_37001437delinsAC , CM000667.1:g.37001436_37001437delinsAC GRCh37
NC_000005.8:g.37037193_37037194delinsAC NCBI36
NG_006987.1:g.129452_129453delinsAC
NG_006987.2:g.129452_129453delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.3664+256_3664+257delinsAC MANE Select ENSP00000282516.8:n.3664+256_3664+257delinsAC
ENST00000652901.1:c.3664+256_3664+257delinsAC ENSP00000499536.1:n.3664+256_3664+257delinsAC
ENST00000282516.12:c.3664+256_3664+257delinsAC ENSP00000282516.8:n.3664+256_3664+257delinsAC
ENST00000448238.2:c.3664+256_3664+257delinsAC ENSP00000406266.2:n.3664+256_3664+257delinsAC
ENST00000621733.1:c.1-63244_1-63243delinsAC ENSP00000480694.1:n.1-63244_1-63243delinsAC
NM_015384.4:c.3664+256_3664+257delinsAC NP_056199.2:n.3664+256_3664+257delinsAC
NM_133433.3:c.3664+256_3664+257delinsAC NP_597677.2:n.3664+256_3664+257delinsAC
XM_005248280.2:c.3664+256_3664+257delinsAC XP_005248337.1:n.3664+256_3664+257delinsAC
XM_005248282.3:c.2920+256_2920+257delinsAC XP_005248339.2:n.2920+256_2920+257delinsAC
XM_006714467.2:c.3664+256_3664+257delinsAC XP_006714530.1:n.3664+256_3664+257delinsAC
XM_006714468.1:c.3466+256_3466+257delinsAC XP_006714531.1:n.3466+256_3466+257delinsAC
XM_011514014.1:c.3283+256_3283+257delinsAC XP_011512316.1:n.3283+256_3283+257delinsAC
XM_011514015.1:c.3664+256_3664+257delinsAC XP_011512317.1:n.3664+256_3664+257delinsAC
XM_005248280.3:c.3664+256_3664+257delinsAC XP_005248337.1:n.3664+256_3664+257delinsAC
XM_005248282.5:c.3004+256_3004+257delinsAC XP_005248339.3:n.3004+256_3004+257delinsAC
XM_006714468.2:c.3466+256_3466+257delinsAC XP_006714531.1:n.3466+256_3466+257delinsAC
XM_017009329.1:c.3664+256_3664+257delinsAC XP_016864818.1:n.3664+256_3664+257delinsAC
XM_017009330.2:c.2047+256_2047+257delinsAC XP_016864819.1:n.2047+256_2047+257delinsAC
XM_017009331.1:c.2038+256_2038+257delinsAC XP_016864820.1:n.2038+256_2038+257delinsAC
NM_133433.4:c.3664+256_3664+257delinsAC MANE Select NP_597677.2:n.3664+256_3664+257delinsAC
NM_015384.5:c.3664+256_3664+257delinsAC NP_056199.2:n.3664+256_3664+257delinsAC