Canonical Allele Identifier: CA2673581596
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37045386_37045387insACTAATGAATTACT , CM000667.2:g.37045386_37045387insACTAATGAATTACT GRCh38
NC_000005.9:g.37045488_37045489insACTAATGAATTACT , CM000667.1:g.37045488_37045489insACTAATGAATTACT GRCh37
NC_000005.8:g.37081245_37081246insACTAATGAATTACT NCBI36
NG_006987.1:g.173504_173505insACTAATGAATTACT
NG_006987.2:g.173504_173505insACTAATGAATTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.6344-57_6344-56insACTAATGAATTACT MANE Select ENSP00000282516.8:n.6344-57_6344-56insACTAATGAATTACT
ENST00000652901.1:c.6344-57_6344-56insACTAATGAATTACT ENSP00000499536.1:n.6344-57_6344-56insACTAATGAATTACT
ENST00000282516.12:c.6344-57_6344-56insACTAATGAATTACT ENSP00000282516.8:n.6344-57_6344-56insACTAATGAATTACT
ENST00000448238.2:c.6344-57_6344-56insACTAATGAATTACT ENSP00000406266.2:n.6344-57_6344-56insACTAATGAATTACT
ENST00000621733.1:c.1-19192_1-19191insACTAATGAATTACT ENSP00000480694.1:n.1-19192_1-19191insACTAATGAATTACT
NM_015384.4:c.6344-57_6344-56insACTAATGAATTACT NP_056199.2:n.6344-57_6344-56insACTAATGAATTACT
NM_133433.3:c.6344-57_6344-56insACTAATGAATTACT NP_597677.2:n.6344-57_6344-56insACTAATGAATTACT
XM_005248280.2:c.6344-57_6344-56insACTAATGAATTACT XP_005248337.1:n.6344-57_6344-56insACTAATGAATTACT
XM_005248282.3:c.5600-57_5600-56insACTAATGAATTACT XP_005248339.2:n.5600-57_5600-56insACTAATGAATTACT
XM_006714467.2:c.6344-57_6344-56insACTAATGAATTACT XP_006714530.1:n.6344-57_6344-56insACTAATGAATTACT
XM_006714468.1:c.6146-57_6146-56insACTAATGAATTACT XP_006714531.1:n.6146-57_6146-56insACTAATGAATTACT
XM_011514014.1:c.5963-57_5963-56insACTAATGAATTACT XP_011512316.1:n.5963-57_5963-56insACTAATGAATTACT
XM_011514015.1:c.6344-57_6344-56insACTAATGAATTACT XP_011512317.1:n.6344-57_6344-56insACTAATGAATTACT
XM_005248280.3:c.6344-57_6344-56insACTAATGAATTACT XP_005248337.1:n.6344-57_6344-56insACTAATGAATTACT
XM_005248282.5:c.5684-57_5684-56insACTAATGAATTACT XP_005248339.3:n.5684-57_5684-56insACTAATGAATTACT
XM_006714468.2:c.6146-57_6146-56insACTAATGAATTACT XP_006714531.1:n.6146-57_6146-56insACTAATGAATTACT
XM_017009329.1:c.6344-57_6344-56insACTAATGAATTACT XP_016864818.1:n.6344-57_6344-56insACTAATGAATTACT
XM_017009330.2:c.4727-57_4727-56insACTAATGAATTACT XP_016864819.1:n.4727-57_4727-56insACTAATGAATTACT
XM_017009331.1:c.4718-57_4718-56insACTAATGAATTACT XP_016864820.1:n.4718-57_4718-56insACTAATGAATTACT
NM_133433.4:c.6344-57_6344-56insACTAATGAATTACT MANE Select NP_597677.2:n.6344-57_6344-56insACTAATGAATTACT
NM_015384.5:c.6344-57_6344-56insACTAATGAATTACT NP_056199.2:n.6344-57_6344-56insACTAATGAATTACT