Canonical Allele Identifier: CA1539571622

Gene: NIPBL

Linked Data

• dbSNP Id: rs1753606458
• gnomAD v4: 5-37052001-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37052001C>T , CM000667.2:g.37052001C>T	GRCh38
NC_000005.9:g.37052103C>T , CM000667.1:g.37052103C>T	GRCh37
NC_000005.8:g.37087860C>T	NCBI36
NG_006987.1:g.180119C>T
NG_006987.2:g.180119C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7062+115C>T MANE Select	ENSP00000282516.8:n.7062+115C>T
ENST00000652901.1:c.7062+115C>T	ENSP00000499536.1:n.7062+115C>T
ENST00000282516.12:c.7062+115C>T	ENSP00000282516.8:n.7062+115C>T
ENST00000448238.2:c.7062+115C>T	ENSP00000406266.2:n.7062+115C>T
ENST00000514335.1:n.944+115C>T
ENST00000621733.1:c.1-12577C>T	ENSP00000480694.1:n.1-12577C>T
NM_015384.4:c.7062+115C>T	NP_056199.2:n.7062+115C>T
NM_133433.3:c.7062+115C>T	NP_597677.2:n.7062+115C>T
XM_005248280.2:c.7062+115C>T	XP_005248337.1:n.7062+115C>T
XM_005248282.3:c.6318+115C>T	XP_005248339.2:n.6318+115C>T
XM_006714467.2:c.7062+115C>T	XP_006714530.1:n.7062+115C>T
XM_006714468.1:c.6864+115C>T	XP_006714531.1:n.6864+115C>T
XM_011514014.1:c.6681+115C>T	XP_011512316.1:n.6681+115C>T
XM_011514015.1:c.7062+115C>T	XP_011512317.1:n.7062+115C>T
XM_005248280.3:c.7062+115C>T	XP_005248337.1:n.7062+115C>T
XM_005248282.5:c.6402+115C>T	XP_005248339.3:n.6402+115C>T
XM_006714468.2:c.6864+115C>T	XP_006714531.1:n.6864+115C>T
XM_017009329.1:c.7062+115C>T	XP_016864818.1:n.7062+115C>T
XM_017009330.2:c.5445+115C>T	XP_016864819.1:n.5445+115C>T
XM_017009331.1:c.5436+115C>T	XP_016864820.1:n.5436+115C>T
NM_133433.4:c.7062+115C>T MANE Select	NP_597677.2:n.7062+115C>T
NM_015384.5:c.7062+115C>T	NP_056199.2:n.7062+115C>T