Canonical Allele Identifier: CA443905075
Gene: NIPBL HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.37020719A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37020617A>T , CM000667.2:g.37020617A>T GRCh38
NC_000005.9:g.37020719A>T , CM000667.1:g.37020719A>T GRCh37
NC_000005.8:g.37056476A>T NCBI36
NG_006987.1:g.148735A>T
NG_006987.2:g.148735A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.5169A>T MANE Select ENSP00000282516.8:p.Arg1723=
ENST00000652901.1:c.5169A>T ENSP00000499536.1:p.Arg1723=
ENST00000282516.12:c.5169A>T ENSP00000282516.8:p.Arg1723=
ENST00000448238.2:c.5169A>T ENSP00000406266.2:p.Arg1723=
ENST00000621733.1:c.1-43961A>T ENSP00000480694.1:n.1-43961A>T
NM_015384.4:c.5169A>T NP_056199.2:p.Arg1723=
NM_133433.3:c.5169A>T NP_597677.2:p.Arg1723=
XM_005248280.2:c.5169A>T XP_005248337.1:p.Arg1723=
XM_005248282.3:c.4425A>T XP_005248339.2:p.Arg1475=
XM_006714467.2:c.5169A>T XP_006714530.1:p.Arg1723=
XM_006714468.1:c.4971A>T XP_006714531.1:p.Arg1657=
XM_011514014.1:c.4788A>T XP_011512316.1:p.Arg1596=
XM_011514015.1:c.5169A>T XP_011512317.1:p.Arg1723=
XM_005248280.3:c.5169A>T XP_005248337.1:p.Arg1723=
XM_005248282.5:c.4509A>T XP_005248339.3:p.Arg1503=
XM_006714468.2:c.4971A>T XP_006714531.1:p.Arg1657=
XM_017009329.1:c.5169A>T XP_016864818.1:p.Arg1723=
XM_017009330.2:c.3552A>T XP_016864819.1:p.Arg1184=
XM_017009331.1:c.3543A>T XP_016864820.1:p.Arg1181=
NM_133433.4:c.5169A>T MANE Select NP_597677.2:p.Arg1723=
NM_015384.5:c.5169A>T NP_056199.2:p.Arg1723=