Canonical Allele Identifier: CA810292123

Gene: NIPBL

Linked Data

• dbSNP Id: rs1290174368
• MyVariant Identifiers: chr5:g.36953702_36953703insT (hg19) ; chr5:g.36953600_36953601insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36953601dup , CM000667.2:g.36953601dup	GRCh38
NC_000005.9:g.36953703dup , CM000667.1:g.36953703dup	GRCh37
NC_000005.8:g.36989460dup	NCBI36
NG_006987.1:g.81719dup
NG_006987.2:g.81719dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.-79-17dup MANE Select	ENSP00000282516.8:n.-79-17dup
ENST00000652901.1:c.-79-17dup	ENSP00000499536.1:n.-79-17dup
ENST00000282516.12:c.-79-17dup	ENSP00000282516.8:n.-79-17dup
ENST00000448238.2:c.-79-17dup	ENSP00000406266.2:n.-79-17dup
ENST00000621733.1:c.-1+76579dup	ENSP00000480694.1:n.-1+76579dup
NM_015384.4:c.-79-17dup	NP_056199.2:n.-79-17dup
NM_133433.3:c.-79-17dup	NP_597677.2:n.-79-17dup
XM_005248280.2:c.-79-17dup	XP_005248337.1:n.-79-17dup
XM_006714467.2:c.-79-17dup	XP_006714530.1:n.-79-17dup
XM_006714468.1:c.-79-17dup	XP_006714531.1:n.-79-17dup
XM_011514014.1:c.-79-17dup	XP_011512316.1:n.-79-17dup
XM_011514015.1:c.-79-17dup	XP_011512317.1:n.-79-17dup
XM_005248280.3:c.-79-17dup	XP_005248337.1:n.-79-17dup
XM_006714468.2:c.-79-17dup	XP_006714531.1:n.-79-17dup
XM_017009329.1:c.-79-17dup	XP_016864818.1:n.-79-17dup
XM_017009331.1:c.-79-17dup	XP_016864820.1:n.-79-17dup
NM_133433.4:c.-79-17dup MANE Select	NP_597677.2:n.-79-17dup
NM_015384.5:c.-79-17dup	NP_056199.2:n.-79-17dup