Canonical Allele Identifier: CA2673573017

Gene: NIPBL

Linked Data

• gnomAD v4: 5-36876823-T-TGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36876823_36876824insGGGGGGGGGGGG , CM000667.2:g.36876823_36876824insGGGGGGGGGGGG	GRCh38
NC_000005.9:g.36876925_36876926insGGGGGGGGGGGG , CM000667.1:g.36876925_36876926insGGGGGGGGGGGG	GRCh37
NC_000005.8:g.36912682_36912683insGGGGGGGGGGGG	NCBI36
NG_006987.1:g.4941_4942insGGGGGGGGGGGG
NG_006987.2:g.4941_4942insGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.-435_-434insGGGGGGGGGGGG MANE Select	ENSP00000282516.8:n.-435_-434insGGGGGGGGGGGG
ENST00000282516.12:c.-435_-434insGGGGGGGGGGGG	ENSP00000282516.8:n.-435_-434insGGGGGGGGGGGG
ENST00000448238.2:c.-435_-434insGGGGGGGGGGGG	ENSP00000406266.2:n.-435_-434insGGGGGGGGGGGG
NM_015384.4:c.-435_-434insGGGGGGGGGGGG	NP_056199.2:n.-435_-434insGGGGGGGGGGGG
NM_133433.3:c.-435_-434insGGGGGGGGGGGG	NP_597677.2:n.-435_-434insGGGGGGGGGGGG
XM_005248280.2:c.-435_-434insGGGGGGGGGGGG	XP_005248337.1:n.-435_-434insGGGGGGGGGGGG
XM_006714467.2:c.-435_-434insGGGGGGGGGGGG	XP_006714530.1:n.-435_-434insGGGGGGGGGGGG
XM_006714468.1:c.-435_-434insGGGGGGGGGGGG	XP_006714531.1:n.-435_-434insGGGGGGGGGGGG
XM_011514014.1:c.-435_-434insGGGGGGGGGGGG	XP_011512316.1:n.-435_-434insGGGGGGGGGGGG
XM_011514015.1:c.-435_-434insGGGGGGGGGGGG	XP_011512317.1:n.-435_-434insGGGGGGGGGGGG
XM_005248280.3:c.-435_-434insGGGGGGGGGGGG	XP_005248337.1:n.-435_-434insGGGGGGGGGGGG
XM_006714468.2:c.-435_-434insGGGGGGGGGGGG	XP_006714531.1:n.-435_-434insGGGGGGGGGGGG
XM_017009329.1:c.-435_-434insGGGGGGGGGGGG	XP_016864818.1:n.-435_-434insGGGGGGGGGGGG
XM_017009331.1:c.-435_-434insGGGGGGGGGGGG	XP_016864820.1:n.-435_-434insGGGGGGGGGGGG
NM_133433.4:c.-435_-434insGGGGGGGGGGGG MANE Select	NP_597677.2:n.-435_-434insGGGGGGGGGGGG
NM_015384.5:c.-435_-434insGGGGGGGGGGGG	NP_056199.2:n.-435_-434insGGGGGGGGGGGG