Canonical Allele Identifier: CA359504200
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37045481C>A , CM000667.2:g.37045481C>A GRCh38
NC_000005.9:g.37045583C>A , CM000667.1:g.37045583C>A GRCh37
NC_000005.8:g.37081340C>A NCBI36
NG_006987.1:g.173599C>A
NG_006987.2:g.173599C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.6382C>A MANE Select ENSP00000282516.8:p.Pro2128Thr
ENST00000652901.1:c.6382C>A ENSP00000499536.1:p.Pro2128Thr
ENST00000282516.12:c.6382C>A ENSP00000282516.8:p.Pro2128Thr
ENST00000448238.2:c.6382C>A ENSP00000406266.2:p.Pro2128Thr
ENST00000621733.1:c.1-19097C>A ENSP00000480694.1:n.1-19097C>A
NM_015384.4:c.6382C>A NP_056199.2:p.Pro2128Thr
NM_133433.3:c.6382C>A NP_597677.2:p.Pro2128Thr
XM_005248280.2:c.6382C>A XP_005248337.1:p.Pro2128Thr
XM_005248282.3:c.5638C>A XP_005248339.2:p.Pro1880Thr
XM_006714467.2:c.6382C>A XP_006714530.1:p.Pro2128Thr
XM_006714468.1:c.6184C>A XP_006714531.1:p.Pro2062Thr
XM_011514014.1:c.6001C>A XP_011512316.1:p.Pro2001Thr
XM_011514015.1:c.6382C>A XP_011512317.1:p.Pro2128Thr
XM_005248280.3:c.6382C>A XP_005248337.1:p.Pro2128Thr
XM_005248282.5:c.5722C>A XP_005248339.3:p.Pro1908Thr
XM_006714468.2:c.6184C>A XP_006714531.1:p.Pro2062Thr
XM_017009329.1:c.6382C>A XP_016864818.1:p.Pro2128Thr
XM_017009330.2:c.4765C>A XP_016864819.1:p.Pro1589Thr
XM_017009331.1:c.4756C>A XP_016864820.1:p.Pro1586Thr
NM_133433.4:c.6382C>A MANE Select NP_597677.2:p.Pro2128Thr
NM_015384.5:c.6382C>A NP_056199.2:p.Pro2128Thr