Canonical Allele Identifier: CA359506133
Gene: NIPBL HGNC NCBI

Linked Data

gnomAD v4: 5-36986031-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36986031G>A , CM000667.2:g.36986031G>A GRCh38
NC_000005.9:g.36986133G>A , CM000667.1:g.36986133G>A GRCh37
NC_000005.8:g.37021890G>A NCBI36
NG_006987.1:g.114149G>A
NG_006987.2:g.114149G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.2851G>A MANE Select ENSP00000282516.8:p.Gly951Ser
ENST00000652901.1:c.2851G>A ENSP00000499536.1:p.Gly951Ser
ENST00000282516.12:c.2851G>A ENSP00000282516.8:p.Gly951Ser
ENST00000448238.2:c.2851G>A ENSP00000406266.2:p.Gly951Ser
ENST00000504430.5:n.2471G>A
ENST00000621733.1:c.1-78547G>A ENSP00000480694.1:n.1-78547G>A
NM_015384.4:c.2851G>A NP_056199.2:p.Gly951Ser
NM_133433.3:c.2851G>A NP_597677.2:p.Gly951Ser
XM_005248280.2:c.2851G>A XP_005248337.1:p.Gly951Ser
XM_005248282.3:c.2107G>A XP_005248339.2:p.Gly703Ser
XM_006714467.2:c.2851G>A XP_006714530.1:p.Gly951Ser
XM_006714468.1:c.2851G>A XP_006714531.1:p.Gly951Ser
XM_011514014.1:c.2851G>A XP_011512316.1:p.Gly951Ser
XM_011514015.1:c.2851G>A XP_011512317.1:p.Gly951Ser
XM_005248280.3:c.2851G>A XP_005248337.1:p.Gly951Ser
XM_005248282.5:c.2191G>A XP_005248339.3:p.Gly731Ser
XM_006714468.2:c.2851G>A XP_006714531.1:p.Gly951Ser
XM_017009329.1:c.2851G>A XP_016864818.1:p.Gly951Ser
XM_017009330.2:c.1234G>A XP_016864819.1:p.Gly412Ser
XM_017009331.1:c.1496-9591G>A XP_016864820.1:n.1496-9591G>A
NM_133433.4:c.2851G>A MANE Select NP_597677.2:p.Gly951Ser
NM_015384.5:c.2851G>A NP_056199.2:p.Gly951Ser