Canonical Allele Identifier: CA359502904
Gene: NIPBL HGNC NCBI

Linked Data

gnomAD v4: 5-36985771-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36985771A>T , CM000667.2:g.36985771A>T GRCh38
NC_000005.9:g.36985873A>T , CM000667.1:g.36985873A>T GRCh37
NC_000005.8:g.37021630A>T NCBI36
NG_006987.1:g.113889A>T
NG_006987.2:g.113889A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.2591A>T MANE Select ENSP00000282516.8:p.Asp864Val
ENST00000652901.1:c.2591A>T ENSP00000499536.1:p.Asp864Val
ENST00000282516.12:c.2591A>T ENSP00000282516.8:p.Asp864Val
ENST00000448238.2:c.2591A>T ENSP00000406266.2:p.Asp864Val
ENST00000504430.5:n.2211A>T
ENST00000621733.1:c.1-78807A>T ENSP00000480694.1:n.1-78807A>T
NM_015384.4:c.2591A>T NP_056199.2:p.Asp864Val
NM_133433.3:c.2591A>T NP_597677.2:p.Asp864Val
XM_005248280.2:c.2591A>T XP_005248337.1:p.Asp864Val
XM_005248282.3:c.1847A>T XP_005248339.2:p.Asp616Val
XM_006714467.2:c.2591A>T XP_006714530.1:p.Asp864Val
XM_006714468.1:c.2591A>T XP_006714531.1:p.Asp864Val
XM_011514014.1:c.2591A>T XP_011512316.1:p.Asp864Val
XM_011514015.1:c.2591A>T XP_011512317.1:p.Asp864Val
XM_005248280.3:c.2591A>T XP_005248337.1:p.Asp864Val
XM_005248282.5:c.1931A>T XP_005248339.3:p.Asp644Val
XM_006714468.2:c.2591A>T XP_006714531.1:p.Asp864Val
XM_017009329.1:c.2591A>T XP_016864818.1:p.Asp864Val
XM_017009330.2:c.974A>T XP_016864819.1:p.Asp325Val
XM_017009331.1:c.1495+9369A>T XP_016864820.1:n.1495+9369A>T
NM_133433.4:c.2591A>T MANE Select NP_597677.2:p.Asp864Val
NM_015384.5:c.2591A>T NP_056199.2:p.Asp864Val