Canonical Allele Identifier: CA1539582148
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36985595T= , CM000667.2:g.36985595T= GRCh38
NC_000005.9:g.36985697T= , CM000667.1:g.36985697T= GRCh37
NC_000005.8:g.37021454T= NCBI36
NG_006987.1:g.113713T=
NG_006987.2:g.113713T=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.2415T= MANE Select ENSP00000282516.8:p.Pro805=
ENST00000652901.1:c.2415T= ENSP00000499536.1:p.Pro805=
ENST00000282516.12:c.2415T= ENSP00000282516.8:p.Pro805=
ENST00000448238.2:c.2415T= ENSP00000406266.2:p.Pro805=
ENST00000504430.5:n.2035T=
ENST00000621733.1:c.1-78983T= ENSP00000480694.1:n.1-78983T=
NM_015384.4:c.2415T= NP_056199.2:p.Pro805=
NM_133433.3:c.2415T= NP_597677.2:p.Pro805=
XM_005248280.2:c.2415T= XP_005248337.1:p.Pro805=
XM_005248282.3:c.1671T= XP_005248339.2:p.Pro557=
XM_006714467.2:c.2415T= XP_006714530.1:p.Pro805=
XM_006714468.1:c.2415T= XP_006714531.1:p.Pro805=
XM_011514014.1:c.2415T= XP_011512316.1:p.Pro805=
XM_011514015.1:c.2415T= XP_011512317.1:p.Pro805=
XM_005248280.3:c.2415T= XP_005248337.1:p.Pro805=
XM_005248282.5:c.1755T= XP_005248339.3:p.Pro585=
XM_006714468.2:c.2415T= XP_006714531.1:p.Pro805=
XM_017009329.1:c.2415T= XP_016864818.1:p.Pro805=
XM_017009330.2:c.798T= XP_016864819.1:p.Pro266=
XM_017009331.1:c.1495+9193T= XP_016864820.1:n.1495+9193T=
NM_133433.4:c.2415T= MANE Select NP_597677.2:p.Pro805=
NM_015384.5:c.2415T= NP_056199.2:p.Pro805=