Canonical Allele Identifier: CA2673550129

Gene: NIPBL

Linked Data

• gnomAD v4: 5-37002653-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37002657dup , CM000667.2:g.37002657dup	GRCh38
NC_000005.9:g.37002759dup , CM000667.1:g.37002759dup	GRCh37
NC_000005.8:g.37038516dup	NCBI36
NG_006987.1:g.130775dup
NG_006987.2:g.130775dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.3665-5dup MANE Select	ENSP00000282516.8:n.3665-5dup
ENST00000652901.1:c.3665-5dup	ENSP00000499536.1:n.3665-5dup
ENST00000282516.12:c.3665-5dup	ENSP00000282516.8:n.3665-5dup
ENST00000448238.2:c.3665-5dup	ENSP00000406266.2:n.3665-5dup
ENST00000621733.1:c.1-61921dup	ENSP00000480694.1:n.1-61921dup
NM_015384.4:c.3665-5dup	NP_056199.2:n.3665-5dup
NM_133433.3:c.3665-5dup	NP_597677.2:n.3665-5dup
XM_005248280.2:c.3665-5dup	XP_005248337.1:n.3665-5dup
XM_005248282.3:c.2921-5dup	XP_005248339.2:n.2921-5dup
XM_006714467.2:c.3665-5dup	XP_006714530.1:n.3665-5dup
XM_006714468.1:c.3467-5dup	XP_006714531.1:n.3467-5dup
XM_011514014.1:c.3284-5dup	XP_011512316.1:n.3284-5dup
XM_011514015.1:c.3665-5dup	XP_011512317.1:n.3665-5dup
XM_005248280.3:c.3665-5dup	XP_005248337.1:n.3665-5dup
XM_005248282.5:c.3005-5dup	XP_005248339.3:n.3005-5dup
XM_006714468.2:c.3467-5dup	XP_006714531.1:n.3467-5dup
XM_017009329.1:c.3665-5dup	XP_016864818.1:n.3665-5dup
XM_017009330.2:c.2048-5dup	XP_016864819.1:n.2048-5dup
XM_017009331.1:c.2039-5dup	XP_016864820.1:n.2039-5dup
NM_133433.4:c.3665-5dup MANE Select	NP_597677.2:n.3665-5dup
NM_015384.5:c.3665-5dup	NP_056199.2:n.3665-5dup