Canonical Allele Identifier: CA2673550883
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37003199_37003201del , CM000667.2:g.37003199_37003201del GRCh38
NC_000005.9:g.37003301_37003303del , CM000667.1:g.37003301_37003303del GRCh37
NC_000005.8:g.37039058_37039060del NCBI36
NG_006987.1:g.131317_131319del
NG_006987.2:g.131317_131319del

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.3769-62_3769-60del MANE Select ENSP00000282516.8:n.3769-62_3769-60del
ENST00000652901.1:c.3769-62_3769-60del ENSP00000499536.1:n.3769-62_3769-60del
ENST00000282516.12:c.3769-62_3769-60del ENSP00000282516.8:n.3769-62_3769-60del
ENST00000448238.2:c.3769-62_3769-60del ENSP00000406266.2:n.3769-62_3769-60del
ENST00000621733.1:c.1-61379_1-61377del ENSP00000480694.1:n.1-61379_1-61377del
NM_015384.4:c.3769-62_3769-60del NP_056199.2:n.3769-62_3769-60del
NM_133433.3:c.3769-62_3769-60del NP_597677.2:n.3769-62_3769-60del
XM_005248280.2:c.3769-62_3769-60del XP_005248337.1:n.3769-62_3769-60del
XM_005248282.3:c.3025-62_3025-60del XP_005248339.2:n.3025-62_3025-60del
XM_006714467.2:c.3769-62_3769-60del XP_006714530.1:n.3769-62_3769-60del
XM_006714468.1:c.3571-62_3571-60del XP_006714531.1:n.3571-62_3571-60del
XM_011514014.1:c.3388-62_3388-60del XP_011512316.1:n.3388-62_3388-60del
XM_011514015.1:c.3769-62_3769-60del XP_011512317.1:n.3769-62_3769-60del
XM_005248280.3:c.3769-62_3769-60del XP_005248337.1:n.3769-62_3769-60del
XM_005248282.5:c.3109-62_3109-60del XP_005248339.3:n.3109-62_3109-60del
XM_006714468.2:c.3571-62_3571-60del XP_006714531.1:n.3571-62_3571-60del
XM_017009329.1:c.3769-62_3769-60del XP_016864818.1:n.3769-62_3769-60del
XM_017009330.2:c.2152-62_2152-60del XP_016864819.1:n.2152-62_2152-60del
XM_017009331.1:c.2143-62_2143-60del XP_016864820.1:n.2143-62_2143-60del
NM_133433.4:c.3769-62_3769-60del MANE Select NP_597677.2:n.3769-62_3769-60del
NM_015384.5:c.3769-62_3769-60del NP_056199.2:n.3769-62_3769-60del