Canonical Allele Identifier: CA2673575002
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37001096_37001137dup , CM000667.2:g.37001096_37001137dup GRCh38
NC_000005.9:g.37001198_37001239dup , CM000667.1:g.37001198_37001239dup GRCh37
NC_000005.8:g.37036955_37036996dup NCBI36
NG_006987.1:g.129214_129255dup
NG_006987.2:g.129214_129255dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.3664+18_3664+59dup MANE Select ENSP00000282516.8:n.3664+18_3664+59dup
ENST00000652901.1:c.3664+18_3664+59dup ENSP00000499536.1:n.3664+18_3664+59dup
ENST00000282516.12:c.3664+18_3664+59dup ENSP00000282516.8:n.3664+18_3664+59dup
ENST00000448238.2:c.3664+18_3664+59dup ENSP00000406266.2:n.3664+18_3664+59dup
ENST00000621733.1:c.1-63482_1-63441dup ENSP00000480694.1:n.1-63482_1-63441dup
NM_015384.4:c.3664+18_3664+59dup NP_056199.2:n.3664+18_3664+59dup
NM_133433.3:c.3664+18_3664+59dup NP_597677.2:n.3664+18_3664+59dup
XM_005248280.2:c.3664+18_3664+59dup XP_005248337.1:n.3664+18_3664+59dup
XM_005248282.3:c.2920+18_2920+59dup XP_005248339.2:n.2920+18_2920+59dup
XM_006714467.2:c.3664+18_3664+59dup XP_006714530.1:n.3664+18_3664+59dup
XM_006714468.1:c.3466+18_3466+59dup XP_006714531.1:n.3466+18_3466+59dup
XM_011514014.1:c.3283+18_3283+59dup XP_011512316.1:n.3283+18_3283+59dup
XM_011514015.1:c.3664+18_3664+59dup XP_011512317.1:n.3664+18_3664+59dup
XM_005248280.3:c.3664+18_3664+59dup XP_005248337.1:n.3664+18_3664+59dup
XM_005248282.5:c.3004+18_3004+59dup XP_005248339.3:n.3004+18_3004+59dup
XM_006714468.2:c.3466+18_3466+59dup XP_006714531.1:n.3466+18_3466+59dup
XM_017009329.1:c.3664+18_3664+59dup XP_016864818.1:n.3664+18_3664+59dup
XM_017009330.2:c.2047+18_2047+59dup XP_016864819.1:n.2047+18_2047+59dup
XM_017009331.1:c.2038+18_2038+59dup XP_016864820.1:n.2038+18_2038+59dup
NM_133433.4:c.3664+18_3664+59dup MANE Select NP_597677.2:n.3664+18_3664+59dup
NM_015384.5:c.3664+18_3664+59dup NP_056199.2:n.3664+18_3664+59dup