Canonical Allele Identifier: CA359487576
Gene: NIPBL HGNC NCBI

Linked Data

ClinVar Variation Id: 521020
dbSNP Id: rs1554015303

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36976342C>T , CM000667.2:g.36976342C>T GRCh38
NC_000005.9:g.36976444C>T , CM000667.1:g.36976444C>T GRCh37
NC_000005.8:g.37012201C>T NCBI36
NG_006987.1:g.104460C>T
NG_006987.2:g.104460C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.1435C>T MANE Select ENSP00000282516.8:p.Arg479Ter
ENST00000652901.1:c.1435C>T ENSP00000499536.1:p.Arg479Ter
ENST00000282516.12:c.1435C>T ENSP00000282516.8:p.Arg479Ter
ENST00000448238.2:c.1435C>T ENSP00000406266.2:p.Arg479Ter
ENST00000504430.5:n.1055C>T
ENST00000621733.1:c.1-88236C>T ENSP00000480694.1:n.1-88236C>T
NM_015384.4:c.1435C>T NP_056199.2:p.Arg479Ter
NM_133433.3:c.1435C>T NP_597677.2:p.Arg479Ter
XM_005248280.2:c.1435C>T XP_005248337.1:p.Arg479Ter
XM_005248282.3:c.691C>T XP_005248339.2:p.Arg231Ter
XM_006714467.2:c.1435C>T XP_006714530.1:p.Arg479Ter
XM_006714468.1:c.1435C>T XP_006714531.1:p.Arg479Ter
XM_011514014.1:c.1435C>T XP_011512316.1:p.Arg479Ter
XM_011514015.1:c.1435C>T XP_011512317.1:p.Arg479Ter
XM_005248280.3:c.1435C>T XP_005248337.1:p.Arg479Ter
XM_005248282.5:c.775C>T XP_005248339.3:p.Arg259Ter
XM_006714468.2:c.1435C>T XP_006714531.1:p.Arg479Ter
XM_017009329.1:c.1435C>T XP_016864818.1:p.Arg479Ter
XM_017009331.1:c.1435C>T XP_016864820.1:p.Arg479Ter
NM_133433.4:c.1435C>T MANE Select NP_597677.2:p.Arg479Ter
NM_015384.5:c.1435C>T NP_056199.2:p.Arg479Ter