Canonical Allele Identifier: CA1539572046
Gene: NIPBL HGNC NCBI

Linked Data

dbSNP Id: rs1753654456
gnomAD v4: 5-37052347-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37052347A>T , CM000667.2:g.37052347A>T GRCh38
NC_000005.9:g.37052449A>T , CM000667.1:g.37052449A>T GRCh37
NC_000005.8:g.37088206A>T NCBI36
NG_006987.1:g.180465A>T
NG_006987.2:g.180465A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.7063-19A>T MANE Select ENSP00000282516.8:n.7063-19A>T
ENST00000652901.1:c.7063-19A>T ENSP00000499536.1:n.7063-19A>T
ENST00000282516.12:c.7063-19A>T ENSP00000282516.8:n.7063-19A>T
ENST00000448238.2:c.7063-19A>T ENSP00000406266.2:n.7063-19A>T
ENST00000514335.1:n.945-19A>T
ENST00000621733.1:c.1-12231A>T ENSP00000480694.1:n.1-12231A>T
NM_015384.4:c.7063-19A>T NP_056199.2:n.7063-19A>T
NM_133433.3:c.7063-19A>T NP_597677.2:n.7063-19A>T
XM_005248280.2:c.7063-19A>T XP_005248337.1:n.7063-19A>T
XM_005248282.3:c.6319-19A>T XP_005248339.2:n.6319-19A>T
XM_006714467.2:c.7063-19A>T XP_006714530.1:n.7063-19A>T
XM_006714468.1:c.6865-19A>T XP_006714531.1:n.6865-19A>T
XM_011514014.1:c.6682-19A>T XP_011512316.1:n.6682-19A>T
XM_011514015.1:c.7063-19A>T XP_011512317.1:n.7063-19A>T
XM_005248280.3:c.7063-19A>T XP_005248337.1:n.7063-19A>T
XM_005248282.5:c.6403-19A>T XP_005248339.3:n.6403-19A>T
XM_006714468.2:c.6865-19A>T XP_006714531.1:n.6865-19A>T
XM_017009329.1:c.7063-19A>T XP_016864818.1:n.7063-19A>T
XM_017009330.2:c.5446-19A>T XP_016864819.1:n.5446-19A>T
XM_017009331.1:c.5437-19A>T XP_016864820.1:n.5437-19A>T
NM_133433.4:c.7063-19A>T MANE Select NP_597677.2:n.7063-19A>T
NM_015384.5:c.7063-19A>T NP_056199.2:n.7063-19A>T