Canonical Allele Identifier: CA2673573043
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36876825_36876826insGGG , CM000667.2:g.36876825_36876826insGGG GRCh38
NC_000005.9:g.36876927_36876928insGGG , CM000667.1:g.36876927_36876928insGGG GRCh37
NC_000005.8:g.36912684_36912685insGGG NCBI36
NG_006987.1:g.4943_4944insGGG
NG_006987.2:g.4943_4944insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.-433_-432insGGG MANE Select ENSP00000282516.8:n.-433_-432insGGG
ENST00000282516.12:c.-433_-432insGGG ENSP00000282516.8:n.-433_-432insGGG
ENST00000448238.2:c.-433_-432insGGG ENSP00000406266.2:n.-433_-432insGGG
NM_015384.4:c.-433_-432insGGG NP_056199.2:n.-433_-432insGGG
NM_133433.3:c.-433_-432insGGG NP_597677.2:n.-433_-432insGGG
XM_005248280.2:c.-433_-432insGGG XP_005248337.1:n.-433_-432insGGG
XM_006714467.2:c.-433_-432insGGG XP_006714530.1:n.-433_-432insGGG
XM_006714468.1:c.-433_-432insGGG XP_006714531.1:n.-433_-432insGGG
XM_011514014.1:c.-433_-432insGGG XP_011512316.1:n.-433_-432insGGG
XM_011514015.1:c.-433_-432insGGG XP_011512317.1:n.-433_-432insGGG
XM_005248280.3:c.-433_-432insGGG XP_005248337.1:n.-433_-432insGGG
XM_006714468.2:c.-433_-432insGGG XP_006714531.1:n.-433_-432insGGG
XM_017009329.1:c.-433_-432insGGG XP_016864818.1:n.-433_-432insGGG
XM_017009331.1:c.-433_-432insGGG XP_016864820.1:n.-433_-432insGGG
NM_133433.4:c.-433_-432insGGG MANE Select NP_597677.2:n.-433_-432insGGG
NM_015384.5:c.-433_-432insGGG NP_056199.2:n.-433_-432insGGG