Canonical Allele Identifier: CA1539618454
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37045421A= , CM000667.2:g.37045421A= GRCh38
NC_000005.9:g.37045523A= , CM000667.1:g.37045523A= GRCh37
NC_000005.8:g.37081280A= NCBI36
NG_006987.1:g.173539A=
NG_006987.2:g.173539A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.6344-22A= MANE Select ENSP00000282516.8:n.6344-22A=
ENST00000652901.1:c.6344-22A= ENSP00000499536.1:n.6344-22A=
ENST00000282516.12:c.6344-22A= ENSP00000282516.8:n.6344-22A=
ENST00000448238.2:c.6344-22A= ENSP00000406266.2:n.6344-22A=
ENST00000621733.1:c.1-19157A= ENSP00000480694.1:n.1-19157A=
NM_015384.4:c.6344-22A= NP_056199.2:n.6344-22A=
NM_133433.3:c.6344-22A= NP_597677.2:n.6344-22A=
XM_005248280.2:c.6344-22A= XP_005248337.1:n.6344-22A=
XM_005248282.3:c.5600-22A= XP_005248339.2:n.5600-22A=
XM_006714467.2:c.6344-22A= XP_006714530.1:n.6344-22A=
XM_006714468.1:c.6146-22A= XP_006714531.1:n.6146-22A=
XM_011514014.1:c.5963-22A= XP_011512316.1:n.5963-22A=
XM_011514015.1:c.6344-22A= XP_011512317.1:n.6344-22A=
XM_005248280.3:c.6344-22A= XP_005248337.1:n.6344-22A=
XM_005248282.5:c.5684-22A= XP_005248339.3:n.5684-22A=
XM_006714468.2:c.6146-22A= XP_006714531.1:n.6146-22A=
XM_017009329.1:c.6344-22A= XP_016864818.1:n.6344-22A=
XM_017009330.2:c.4727-22A= XP_016864819.1:n.4727-22A=
XM_017009331.1:c.4718-22A= XP_016864820.1:n.4718-22A=
NM_133433.4:c.6344-22A= MANE Select NP_597677.2:n.6344-22A=
NM_015384.5:c.6344-22A= NP_056199.2:n.6344-22A=