Canonical Allele Identifier: CA1539601032
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37000513C= , CM000667.2:g.37000513C= GRCh38
NC_000005.9:g.37000615C= , CM000667.1:g.37000615C= GRCh37
NC_000005.8:g.37036372C= NCBI36
NG_006987.1:g.128631C=
NG_006987.2:g.128631C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.3445C= MANE Select ENSP00000282516.8:p.Arg1149=
ENST00000652901.1:c.3445C= ENSP00000499536.1:p.Arg1149=
ENST00000282516.12:c.3445C= ENSP00000282516.8:p.Arg1149=
ENST00000448238.2:c.3445C= ENSP00000406266.2:p.Arg1149=
ENST00000621733.1:c.1-64065C= ENSP00000480694.1:n.1-64065C=
NM_015384.4:c.3445C= NP_056199.2:p.Arg1149=
NM_133433.3:c.3445C= NP_597677.2:p.Arg1149=
XM_005248280.2:c.3445C= XP_005248337.1:p.Arg1149=
XM_005248282.3:c.2701C= XP_005248339.2:p.Arg901=
XM_006714467.2:c.3445C= XP_006714530.1:p.Arg1149=
XM_006714468.1:c.3305-304C= XP_006714531.1:n.3305-304C=
XM_011514014.1:c.3122-304C= XP_011512316.1:n.3122-304C=
XM_011514015.1:c.3445C= XP_011512317.1:p.Arg1149=
XM_005248280.3:c.3445C= XP_005248337.1:p.Arg1149=
XM_005248282.5:c.2785C= XP_005248339.3:p.Arg929=
XM_006714468.2:c.3305-304C= XP_006714531.1:n.3305-304C=
XM_017009329.1:c.3445C= XP_016864818.1:p.Arg1149=
XM_017009330.2:c.1828C= XP_016864819.1:p.Arg610=
XM_017009331.1:c.1819C= XP_016864820.1:p.Arg607=
NM_133433.4:c.3445C= MANE Select NP_597677.2:p.Arg1149=
NM_015384.5:c.3445C= NP_056199.2:p.Arg1149=