Canonical Allele Identifier: CA359483119

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37016262G>T (hg19) ; chr5:g.37016160G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37016160G>T , CM000667.2:g.37016160G>T	GRCh38
NC_000005.9:g.37016262G>T , CM000667.1:g.37016262G>T	GRCh37
NC_000005.8:g.37052019G>T	NCBI36
NG_006987.1:g.144278G>T
NG_006987.2:g.144278G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4766G>T MANE Select	ENSP00000282516.8:p.Gly1589Val
ENST00000652901.1:c.4766G>T	ENSP00000499536.1:p.Gly1589Val
ENST00000282516.12:c.4766G>T	ENSP00000282516.8:p.Gly1589Val
ENST00000448238.2:c.4766G>T	ENSP00000406266.2:p.Gly1589Val
ENST00000621733.1:c.1-48418G>T	ENSP00000480694.1:n.1-48418G>T
NM_015384.4:c.4766G>T	NP_056199.2:p.Gly1589Val
NM_133433.3:c.4766G>T	NP_597677.2:p.Gly1589Val
XM_005248280.2:c.4766G>T	XP_005248337.1:p.Gly1589Val
XM_005248282.3:c.4022G>T	XP_005248339.2:p.Gly1341Val
XM_006714467.2:c.4766G>T	XP_006714530.1:p.Gly1589Val
XM_006714468.1:c.4568G>T	XP_006714531.1:p.Gly1523Val
XM_011514014.1:c.4385G>T	XP_011512316.1:p.Gly1462Val
XM_011514015.1:c.4766G>T	XP_011512317.1:p.Gly1589Val
XM_005248280.3:c.4766G>T	XP_005248337.1:p.Gly1589Val
XM_005248282.5:c.4106G>T	XP_005248339.3:p.Gly1369Val
XM_006714468.2:c.4568G>T	XP_006714531.1:p.Gly1523Val
XM_017009329.1:c.4766G>T	XP_016864818.1:p.Gly1589Val
XM_017009330.2:c.3149G>T	XP_016864819.1:p.Gly1050Val
XM_017009331.1:c.3140G>T	XP_016864820.1:p.Gly1047Val
NM_133433.4:c.4766G>T MANE Select	NP_597677.2:p.Gly1589Val
NM_015384.5:c.4766G>T	NP_056199.2:p.Gly1589Val