Canonical Allele Identifier: CA1075109195
Gene: NIPBL HGNC NCBI

Linked Data

dbSNP Id: rs1746726168

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37000952_37000956del , CM000667.2:g.37000952_37000956del GRCh38
NC_000005.9:g.37001054_37001058del , CM000667.1:g.37001054_37001058del GRCh37
NC_000005.8:g.37036811_37036815del NCBI36
NG_006987.1:g.129070_129074del
NG_006987.2:g.129070_129074del

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.3575-37_3575-33del MANE Select ENSP00000282516.8:n.3575-37_3575-33del
ENST00000652901.1:c.3575-37_3575-33del ENSP00000499536.1:n.3575-37_3575-33del
ENST00000282516.12:c.3575-37_3575-33del ENSP00000282516.8:n.3575-37_3575-33del
ENST00000448238.2:c.3575-37_3575-33del ENSP00000406266.2:n.3575-37_3575-33del
ENST00000621733.1:c.1-63626_1-63622del ENSP00000480694.1:n.1-63626_1-63622del
NM_015384.4:c.3575-37_3575-33del NP_056199.2:n.3575-37_3575-33del
NM_133433.3:c.3575-37_3575-33del NP_597677.2:n.3575-37_3575-33del
XM_005248280.2:c.3575-37_3575-33del XP_005248337.1:n.3575-37_3575-33del
XM_005248282.3:c.2831-37_2831-33del XP_005248339.2:n.2831-37_2831-33del
XM_006714467.2:c.3575-37_3575-33del XP_006714530.1:n.3575-37_3575-33del
XM_006714468.1:c.3377-37_3377-33del XP_006714531.1:n.3377-37_3377-33del
XM_011514014.1:c.3194-37_3194-33del XP_011512316.1:n.3194-37_3194-33del
XM_011514015.1:c.3575-37_3575-33del XP_011512317.1:n.3575-37_3575-33del
XM_005248280.3:c.3575-37_3575-33del XP_005248337.1:n.3575-37_3575-33del
XM_005248282.5:c.2915-37_2915-33del XP_005248339.3:n.2915-37_2915-33del
XM_006714468.2:c.3377-37_3377-33del XP_006714531.1:n.3377-37_3377-33del
XM_017009329.1:c.3575-37_3575-33del XP_016864818.1:n.3575-37_3575-33del
XM_017009330.2:c.1958-37_1958-33del XP_016864819.1:n.1958-37_1958-33del
XM_017009331.1:c.1949-37_1949-33del XP_016864820.1:n.1949-37_1949-33del
NM_133433.4:c.3575-37_3575-33del MANE Select NP_597677.2:n.3575-37_3575-33del
NM_015384.5:c.3575-37_3575-33del NP_056199.2:n.3575-37_3575-33del