Canonical Allele Identifier: CA2673552145
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36958001_36958002insC , CM000667.2:g.36958001_36958002insC GRCh38
NC_000005.9:g.36958103_36958104insC , CM000667.1:g.36958103_36958104insC GRCh37
NC_000005.8:g.36993860_36993861insC NCBI36
NG_006987.1:g.86119_86120insC
NG_006987.2:g.86119_86120insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.231-103_231-102insC MANE Select ENSP00000282516.8:n.231-103_231-102insC
ENST00000652901.1:c.231-103_231-102insC ENSP00000499536.1:n.231-103_231-102insC
ENST00000282516.12:c.231-103_231-102insC ENSP00000282516.8:n.231-103_231-102insC
ENST00000448238.2:c.231-103_231-102insC ENSP00000406266.2:n.231-103_231-102insC
ENST00000505998.5:n.210-103_210-102insC
ENST00000621733.1:c.-1+80979_-1+80980insC ENSP00000480694.1:n.-1+80979_-1+80980insC
NM_015384.4:c.231-103_231-102insC NP_056199.2:n.231-103_231-102insC
NM_133433.3:c.231-103_231-102insC NP_597677.2:n.231-103_231-102insC
XM_005248280.2:c.231-103_231-102insC XP_005248337.1:n.231-103_231-102insC
XM_006714467.2:c.231-103_231-102insC XP_006714530.1:n.231-103_231-102insC
XM_006714468.1:c.231-103_231-102insC XP_006714531.1:n.231-103_231-102insC
XM_011514014.1:c.231-103_231-102insC XP_011512316.1:n.231-103_231-102insC
XM_011514015.1:c.231-103_231-102insC XP_011512317.1:n.231-103_231-102insC
XM_005248280.3:c.231-103_231-102insC XP_005248337.1:n.231-103_231-102insC
XM_006714468.2:c.231-103_231-102insC XP_006714531.1:n.231-103_231-102insC
XM_017009329.1:c.231-103_231-102insC XP_016864818.1:n.231-103_231-102insC
XM_017009331.1:c.231-103_231-102insC XP_016864820.1:n.231-103_231-102insC
NM_133433.4:c.231-103_231-102insC MANE Select NP_597677.2:n.231-103_231-102insC
NM_015384.5:c.231-103_231-102insC NP_056199.2:n.231-103_231-102insC