Canonical Allele Identifier: CA1539582574
Gene: NIPBL HGNC NCBI

Linked Data

dbSNP Id: rs1754552844

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37060498G>A , CM000667.2:g.37060498G>A GRCh38
NC_000005.9:g.37060600G>A , CM000667.1:g.37060600G>A GRCh37
NC_000005.8:g.37096357G>A NCBI36
NG_006987.1:g.188616G>A
NG_006987.2:g.188616G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.7686-346G>A MANE Select ENSP00000282516.8:n.7686-346G>A
ENST00000652901.1:c.7539-346G>A ENSP00000499536.1:n.7539-346G>A
ENST00000282516.12:c.7686-346G>A ENSP00000282516.8:n.7686-346G>A
ENST00000448238.2:c.7686-346G>A ENSP00000406266.2:n.7686-346G>A
ENST00000513819.1:c.263+1333G>A ENSP00000421504.1:n.263+1333G>A
ENST00000514335.1:n.1568-346G>A
ENST00000621733.1:c.1-4080G>A ENSP00000480694.1:n.1-4080G>A
NM_015384.4:c.7686-346G>A NP_056199.2:n.7686-346G>A
NM_133433.3:c.7686-346G>A NP_597677.2:n.7686-346G>A
XM_005248280.2:c.7686-346G>A XP_005248337.1:n.7686-346G>A
XM_005248282.3:c.6942-346G>A XP_005248339.2:n.6942-346G>A
XM_006714467.2:c.7539-346G>A XP_006714530.1:n.7539-346G>A
XM_006714468.1:c.7488-346G>A XP_006714531.1:n.7488-346G>A
XM_011514014.1:c.7305-346G>A XP_011512316.1:n.7305-346G>A
XM_011514015.1:c.7264-346G>A XP_011512317.1:n.7264-346G>A
XM_005248280.3:c.7686-346G>A XP_005248337.1:n.7686-346G>A
XM_005248282.5:c.7026-346G>A XP_005248339.3:n.7026-346G>A
XM_006714468.2:c.7488-346G>A XP_006714531.1:n.7488-346G>A
XM_017009329.1:c.7539-346G>A XP_016864818.1:n.7539-346G>A
XM_017009330.2:c.6069-346G>A XP_016864819.1:n.6069-346G>A
XM_017009331.1:c.6060-346G>A XP_016864820.1:n.6060-346G>A
NM_133433.4:c.7686-346G>A MANE Select NP_597677.2:n.7686-346G>A
NM_015384.5:c.7686-346G>A NP_056199.2:n.7686-346G>A