Canonical Allele Identifier: CA359519004

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37061078C>G (hg19) ; chr5:g.37060976C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37060976C>G , CM000667.2:g.37060976C>G	GRCh38
NC_000005.9:g.37061078C>G , CM000667.1:g.37061078C>G	GRCh37
NC_000005.8:g.37096835C>G	NCBI36
NG_006987.1:g.189094C>G
NG_006987.2:g.189094C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7818C>G MANE Select	ENSP00000282516.8:p.Ile2606Met
ENST00000652901.1:c.7671C>G	ENSP00000499536.1:p.Ile2557Met
ENST00000282516.12:c.7818C>G	ENSP00000282516.8:p.Ile2606Met
ENST00000448238.2:c.7818C>G	ENSP00000406266.2:p.Ile2606Met
ENST00000513819.1:c.263+1811C>G	ENSP00000421504.1:n.263+1811C>G
ENST00000514335.1:n.1700C>G
ENST00000621733.1:c.1-3602C>G	ENSP00000480694.1:n.1-3602C>G
NM_015384.4:c.7818C>G	NP_056199.2:p.Ile2606Met
NM_133433.3:c.7818C>G	NP_597677.2:p.Ile2606Met
XM_005248280.2:c.7818C>G	XP_005248337.1:p.Ile2606Met
XM_005248282.3:c.7074C>G	XP_005248339.2:p.Ile2358Met
XM_006714467.2:c.7671C>G	XP_006714530.1:p.Ile2557Met
XM_006714468.1:c.7620C>G	XP_006714531.1:p.Ile2540Met
XM_011514014.1:c.7437C>G	XP_011512316.1:p.Ile2479Met
XM_005248280.3:c.7818C>G	XP_005248337.1:p.Ile2606Met
XM_005248282.5:c.7158C>G	XP_005248339.3:p.Ile2386Met
XM_006714468.2:c.7620C>G	XP_006714531.1:p.Ile2540Met
XM_017009329.1:c.7671C>G	XP_016864818.1:p.Ile2557Met
XM_017009330.2:c.6201C>G	XP_016864819.1:p.Ile2067Met
XM_017009331.1:c.6192C>G	XP_016864820.1:p.Ile2064Met
NM_133433.4:c.7818C>G MANE Select	NP_597677.2:p.Ile2606Met
NM_015384.5:c.7818C>G	NP_056199.2:p.Ile2606Met