Canonical Allele Identifier: CA272038
Gene: NIPBL HGNC NCBI

Linked Data

ClinVar Variation Id: 159067
ClinVar RCV Id: RCV000146560
dbSNP Id: rs587783912
MyVariant Identifiers: chr5:g.36986185del (hg19) chr5:g.36986083del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36986083del , CM000667.2:g.36986083del GRCh38
NC_000005.9:g.36986185del , CM000667.1:g.36986185del GRCh37
NC_000005.8:g.37021942del NCBI36
NG_006987.1:g.114201del
NG_006987.2:g.114201del

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.2903del MANE Select ENSP00000282516.8:p.Asn968MetfsTer11
ENST00000652901.1:c.2903del ENSP00000499536.1:p.Asn968MetfsTer11
ENST00000282516.12:c.2903del ENSP00000282516.8:p.Asn968MetfsTer11
ENST00000448238.2:c.2903del ENSP00000406266.2:p.Asn968MetfsTer11
ENST00000504430.5:n.2523del
ENST00000621733.1:c.1-78495del ENSP00000480694.1:n.1-78495del
NM_015384.4:c.2903del NP_056199.2:p.Asn968MetfsTer11
NM_133433.3:c.2903del NP_597677.2:p.Asn968MetfsTer11
XM_005248280.2:c.2903del XP_005248337.1:p.Asn968MetfsTer11
XM_005248282.3:c.2159del XP_005248339.2:p.Asn720MetfsTer11
XM_006714467.2:c.2903del XP_006714530.1:p.Asn968MetfsTer11
XM_006714468.1:c.2903del XP_006714531.1:p.Asn968MetfsTer11
XM_011514014.1:c.2903del XP_011512316.1:p.Asn968MetfsTer11
XM_011514015.1:c.2903del XP_011512317.1:p.Asn968MetfsTer11
XM_005248280.3:c.2903del XP_005248337.1:p.Asn968MetfsTer11
XM_005248282.5:c.2243del XP_005248339.3:p.Asn748MetfsTer11
XM_006714468.2:c.2903del XP_006714531.1:p.Asn968MetfsTer11
XM_017009329.1:c.2903del XP_016864818.1:p.Asn968MetfsTer11
XM_017009330.2:c.1286del XP_016864819.1:p.Asn429MetfsTer11
XM_017009331.1:c.1496-9539del XP_016864820.1:n.1496-9539del
NM_133433.4:c.2903del MANE Select NP_597677.2:p.Asn968MetfsTer11
NM_015384.5:c.2903del NP_056199.2:p.Asn968MetfsTer11
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