Canonical Allele Identifier: CA443907006
Gene: NIPBL HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.37045690C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37045588C>A , CM000667.2:g.37045588C>A GRCh38
NC_000005.9:g.37045690C>A , CM000667.1:g.37045690C>A GRCh37
NC_000005.8:g.37081447C>A NCBI36
NG_006987.1:g.173706C>A
NG_006987.2:g.173706C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.6489C>A MANE Select ENSP00000282516.8:p.Gly2163=
ENST00000652901.1:c.6489C>A ENSP00000499536.1:p.Gly2163=
ENST00000282516.12:c.6489C>A ENSP00000282516.8:p.Gly2163=
ENST00000448238.2:c.6489C>A ENSP00000406266.2:p.Gly2163=
ENST00000621733.1:c.1-18990C>A ENSP00000480694.1:n.1-18990C>A
NM_015384.4:c.6489C>A NP_056199.2:p.Gly2163=
NM_133433.3:c.6489C>A NP_597677.2:p.Gly2163=
XM_005248280.2:c.6489C>A XP_005248337.1:p.Gly2163=
XM_005248282.3:c.5745C>A XP_005248339.2:p.Gly1915=
XM_006714467.2:c.6489C>A XP_006714530.1:p.Gly2163=
XM_006714468.1:c.6291C>A XP_006714531.1:p.Gly2097=
XM_011514014.1:c.6108C>A XP_011512316.1:p.Gly2036=
XM_011514015.1:c.6489C>A XP_011512317.1:p.Gly2163=
XM_005248280.3:c.6489C>A XP_005248337.1:p.Gly2163=
XM_005248282.5:c.5829C>A XP_005248339.3:p.Gly1943=
XM_006714468.2:c.6291C>A XP_006714531.1:p.Gly2097=
XM_017009329.1:c.6489C>A XP_016864818.1:p.Gly2163=
XM_017009330.2:c.4872C>A XP_016864819.1:p.Gly1624=
XM_017009331.1:c.4863C>A XP_016864820.1:p.Gly1621=
NM_133433.4:c.6489C>A MANE Select NP_597677.2:p.Gly2163=
NM_015384.5:c.6489C>A NP_056199.2:p.Gly2163=