Canonical Allele Identifier: CA359513322

Gene: NIPBL

Linked Data

• gnomAD v4: 5-36995633-C-A
• MyVariant Identifiers: chr5:g.36995735C>A (hg19) ; chr5:g.36995633C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36995633C>A , CM000667.2:g.36995633C>A	GRCh38
NC_000005.9:g.36995735C>A , CM000667.1:g.36995735C>A	GRCh37
NC_000005.8:g.37031492C>A	NCBI36
NG_006987.1:g.123751C>A
NG_006987.2:g.123751C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.3133C>A MANE Select	ENSP00000282516.8:p.Gln1045Lys
ENST00000652901.1:c.3133C>A	ENSP00000499536.1:p.Gln1045Lys
ENST00000282516.12:c.3133C>A	ENSP00000282516.8:p.Gln1045Lys
ENST00000448238.2:c.3133C>A	ENSP00000406266.2:p.Gln1045Lys
ENST00000503274.1:n.484C>A
ENST00000504430.5:n.2753C>A
ENST00000621733.1:c.1-68945C>A	ENSP00000480694.1:n.1-68945C>A
NM_015384.4:c.3133C>A	NP_056199.2:p.Gln1045Lys
NM_133433.3:c.3133C>A	NP_597677.2:p.Gln1045Lys
XM_005248280.2:c.3133C>A	XP_005248337.1:p.Gln1045Lys
XM_005248282.3:c.2389C>A	XP_005248339.2:p.Gln797Lys
XM_006714467.2:c.3133C>A	XP_006714530.1:p.Gln1045Lys
XM_006714468.1:c.3133C>A	XP_006714531.1:p.Gln1045Lys
XM_011514014.1:c.3122-5184C>A	XP_011512316.1:n.3122-5184C>A
XM_011514015.1:c.3133C>A	XP_011512317.1:p.Gln1045Lys
XM_005248280.3:c.3133C>A	XP_005248337.1:p.Gln1045Lys
XM_005248282.5:c.2473C>A	XP_005248339.3:p.Gln825Lys
XM_006714468.2:c.3133C>A	XP_006714531.1:p.Gln1045Lys
XM_017009329.1:c.3133C>A	XP_016864818.1:p.Gln1045Lys
XM_017009330.2:c.1516C>A	XP_016864819.1:p.Gln506Lys
XM_017009331.1:c.1507C>A	XP_016864820.1:p.Gln503Lys
NM_133433.4:c.3133C>A MANE Select	NP_597677.2:p.Gln1045Lys
NM_015384.5:c.3133C>A	NP_056199.2:p.Gln1045Lys