Canonical Allele Identifier: CA2673573052

Gene: NIPBL

Linked Data

• gnomAD v4: 5-36876826-C-CGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36876826_36876827insGGG , CM000667.2:g.36876826_36876827insGGG	GRCh38
NC_000005.9:g.36876928_36876929insGGG , CM000667.1:g.36876928_36876929insGGG	GRCh37
NC_000005.8:g.36912685_36912686insGGG	NCBI36
NG_006987.1:g.4944_4945insGGG
NG_006987.2:g.4944_4945insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.-432_-431insGGG MANE Select	ENSP00000282516.8:n.-432_-431insGGG
ENST00000282516.12:c.-432_-431insGGG	ENSP00000282516.8:n.-432_-431insGGG
ENST00000448238.2:c.-432_-431insGGG	ENSP00000406266.2:n.-432_-431insGGG
NM_015384.4:c.-432_-431insGGG	NP_056199.2:n.-432_-431insGGG
NM_133433.3:c.-432_-431insGGG	NP_597677.2:n.-432_-431insGGG
XM_005248280.2:c.-432_-431insGGG	XP_005248337.1:n.-432_-431insGGG
XM_006714467.2:c.-432_-431insGGG	XP_006714530.1:n.-432_-431insGGG
XM_006714468.1:c.-432_-431insGGG	XP_006714531.1:n.-432_-431insGGG
XM_011514014.1:c.-432_-431insGGG	XP_011512316.1:n.-432_-431insGGG
XM_011514015.1:c.-432_-431insGGG	XP_011512317.1:n.-432_-431insGGG
XM_005248280.3:c.-432_-431insGGG	XP_005248337.1:n.-432_-431insGGG
XM_006714468.2:c.-432_-431insGGG	XP_006714531.1:n.-432_-431insGGG
XM_017009329.1:c.-432_-431insGGG	XP_016864818.1:n.-432_-431insGGG
XM_017009331.1:c.-432_-431insGGG	XP_016864820.1:n.-432_-431insGGG
NM_133433.4:c.-432_-431insGGG MANE Select	NP_597677.2:n.-432_-431insGGG
NM_015384.5:c.-432_-431insGGG	NP_056199.2:n.-432_-431insGGG