Canonical Allele Identifier: CA1539618607
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37045590A= , CM000667.2:g.37045590A= GRCh38
NC_000005.9:g.37045692A= , CM000667.1:g.37045692A= GRCh37
NC_000005.8:g.37081449A= NCBI36
NG_006987.1:g.173708A=
NG_006987.2:g.173708A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.6491A= MANE Select ENSP00000282516.8:p.Asn2164=
ENST00000652901.1:c.6491A= ENSP00000499536.1:p.Asn2164=
ENST00000282516.12:c.6491A= ENSP00000282516.8:p.Asn2164=
ENST00000448238.2:c.6491A= ENSP00000406266.2:p.Asn2164=
ENST00000621733.1:c.1-18988A= ENSP00000480694.1:n.1-18988A=
NM_015384.4:c.6491A= NP_056199.2:p.Asn2164=
NM_133433.3:c.6491A= NP_597677.2:p.Asn2164=
XM_005248280.2:c.6491A= XP_005248337.1:p.Asn2164=
XM_005248282.3:c.5747A= XP_005248339.2:p.Asn1916=
XM_006714467.2:c.6491A= XP_006714530.1:p.Asn2164=
XM_006714468.1:c.6293A= XP_006714531.1:p.Asn2098=
XM_011514014.1:c.6110A= XP_011512316.1:p.Asn2037=
XM_011514015.1:c.6491A= XP_011512317.1:p.Asn2164=
XM_005248280.3:c.6491A= XP_005248337.1:p.Asn2164=
XM_005248282.5:c.5831A= XP_005248339.3:p.Asn1944=
XM_006714468.2:c.6293A= XP_006714531.1:p.Asn2098=
XM_017009329.1:c.6491A= XP_016864818.1:p.Asn2164=
XM_017009330.2:c.4874A= XP_016864819.1:p.Asn1625=
XM_017009331.1:c.4865A= XP_016864820.1:p.Asn1622=
NM_133433.4:c.6491A= MANE Select NP_597677.2:p.Asn2164=
NM_015384.5:c.6491A= NP_056199.2:p.Asn2164=