Canonical Allele Identifier: CA1539571027

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36953402_36953405delinsATAG , CM000667.2:g.36953402_36953405delinsATAG	GRCh38
NC_000005.9:g.36953504_36953507delinsATAG , CM000667.1:g.36953504_36953507delinsATAG	GRCh37
NC_000005.8:g.36989261_36989264delinsATAG	NCBI36
NG_006987.1:g.81520_81523delinsATAG
NG_006987.2:g.81520_81523delinsATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.-79-216_-79-213delinsATAG MANE Select	ENSP00000282516.8:n.-79-216_-79-213delinsATAG
ENST00000652901.1:c.-79-216_-79-213delinsATAG	ENSP00000499536.1:n.-79-216_-79-213delinsATAG
ENST00000282516.12:c.-79-216_-79-213delinsATAG	ENSP00000282516.8:n.-79-216_-79-213delinsATAG
ENST00000448238.2:c.-79-216_-79-213delinsATAG	ENSP00000406266.2:n.-79-216_-79-213delinsATAG
ENST00000621733.1:c.-1+76380_-1+76383delinsATAG	ENSP00000480694.1:n.-1+76380_-1+76383delinsATAG
NM_015384.4:c.-79-216_-79-213delinsATAG	NP_056199.2:n.-79-216_-79-213delinsATAG
NM_133433.3:c.-79-216_-79-213delinsATAG	NP_597677.2:n.-79-216_-79-213delinsATAG
XM_005248280.2:c.-79-216_-79-213delinsATAG	XP_005248337.1:n.-79-216_-79-213delinsATAG
XM_006714467.2:c.-79-216_-79-213delinsATAG	XP_006714530.1:n.-79-216_-79-213delinsATAG
XM_006714468.1:c.-79-216_-79-213delinsATAG	XP_006714531.1:n.-79-216_-79-213delinsATAG
XM_011514014.1:c.-79-216_-79-213delinsATAG	XP_011512316.1:n.-79-216_-79-213delinsATAG
XM_011514015.1:c.-79-216_-79-213delinsATAG	XP_011512317.1:n.-79-216_-79-213delinsATAG
XM_005248280.3:c.-79-216_-79-213delinsATAG	XP_005248337.1:n.-79-216_-79-213delinsATAG
XM_006714468.2:c.-79-216_-79-213delinsATAG	XP_006714531.1:n.-79-216_-79-213delinsATAG
XM_017009329.1:c.-79-216_-79-213delinsATAG	XP_016864818.1:n.-79-216_-79-213delinsATAG
XM_017009331.1:c.-79-216_-79-213delinsATAG	XP_016864820.1:n.-79-216_-79-213delinsATAG
NM_133433.4:c.-79-216_-79-213delinsATAG MANE Select	NP_597677.2:n.-79-216_-79-213delinsATAG
NM_015384.5:c.-79-216_-79-213delinsATAG	NP_056199.2:n.-79-216_-79-213delinsATAG