Canonical Allele Identifier: CA1539569009
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36975862C= , CM000667.2:g.36975862C= GRCh38
NC_000005.9:g.36975964C= , CM000667.1:g.36975964C= GRCh37
NC_000005.8:g.37011721C= NCBI36
NG_006987.1:g.103980C=
NG_006987.2:g.103980C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.955C= MANE Select ENSP00000282516.8:p.Pro319=
ENST00000652901.1:c.955C= ENSP00000499536.1:p.Pro319=
ENST00000282516.12:c.955C= ENSP00000282516.8:p.Pro319=
ENST00000448238.2:c.955C= ENSP00000406266.2:p.Pro319=
ENST00000504430.5:n.575C=
ENST00000505998.5:n.934C=
ENST00000621733.1:c.1-88716C= ENSP00000480694.1:n.1-88716C=
NM_015384.4:c.955C= NP_056199.2:p.Pro319=
NM_133433.3:c.955C= NP_597677.2:p.Pro319=
XM_005248280.2:c.955C= XP_005248337.1:p.Pro319=
XM_005248282.3:c.211C= XP_005248339.2:p.Pro71=
XM_006714467.2:c.955C= XP_006714530.1:p.Pro319=
XM_006714468.1:c.955C= XP_006714531.1:p.Pro319=
XM_011514014.1:c.955C= XP_011512316.1:p.Pro319=
XM_011514015.1:c.955C= XP_011512317.1:p.Pro319=
XM_005248280.3:c.955C= XP_005248337.1:p.Pro319=
XM_005248282.5:c.295C= XP_005248339.3:p.Pro99=
XM_006714468.2:c.955C= XP_006714531.1:p.Pro319=
XM_017009329.1:c.955C= XP_016864818.1:p.Pro319=
XM_017009331.1:c.955C= XP_016864820.1:p.Pro319=
NM_133433.4:c.955C= MANE Select NP_597677.2:p.Pro319=
NM_015384.5:c.955C= NP_056199.2:p.Pro319=