Canonical Allele Identifier: CA1539618304

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37045229_37045231delinsCTG , CM000667.2:g.37045229_37045231delinsCTG	GRCh38
NC_000005.9:g.37045331_37045333delinsCTG , CM000667.1:g.37045331_37045333delinsCTG	GRCh37
NC_000005.8:g.37081088_37081090delinsCTG	NCBI36
NG_006987.1:g.173347_173349delinsCTG
NG_006987.2:g.173347_173349delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.6344-214_6344-212delinsCTG MANE Select	ENSP00000282516.8:n.6344-214_6344-212delinsCTG
ENST00000652901.1:c.6344-214_6344-212delinsCTG	ENSP00000499536.1:n.6344-214_6344-212delinsCTG
ENST00000282516.12:c.6344-214_6344-212delinsCTG	ENSP00000282516.8:n.6344-214_6344-212delinsCTG
ENST00000448238.2:c.6344-214_6344-212delinsCTG	ENSP00000406266.2:n.6344-214_6344-212delinsCTG
ENST00000621733.1:c.1-19349_1-19347delinsCTG	ENSP00000480694.1:n.1-19349_1-19347delinsCTG
NM_015384.4:c.6344-214_6344-212delinsCTG	NP_056199.2:n.6344-214_6344-212delinsCTG
NM_133433.3:c.6344-214_6344-212delinsCTG	NP_597677.2:n.6344-214_6344-212delinsCTG
XM_005248280.2:c.6344-214_6344-212delinsCTG	XP_005248337.1:n.6344-214_6344-212delinsCTG
XM_005248282.3:c.5600-214_5600-212delinsCTG	XP_005248339.2:n.5600-214_5600-212delinsCTG
XM_006714467.2:c.6344-214_6344-212delinsCTG	XP_006714530.1:n.6344-214_6344-212delinsCTG
XM_006714468.1:c.6146-214_6146-212delinsCTG	XP_006714531.1:n.6146-214_6146-212delinsCTG
XM_011514014.1:c.5963-214_5963-212delinsCTG	XP_011512316.1:n.5963-214_5963-212delinsCTG
XM_011514015.1:c.6344-214_6344-212delinsCTG	XP_011512317.1:n.6344-214_6344-212delinsCTG
XM_005248280.3:c.6344-214_6344-212delinsCTG	XP_005248337.1:n.6344-214_6344-212delinsCTG
XM_005248282.5:c.5684-214_5684-212delinsCTG	XP_005248339.3:n.5684-214_5684-212delinsCTG
XM_006714468.2:c.6146-214_6146-212delinsCTG	XP_006714531.1:n.6146-214_6146-212delinsCTG
XM_017009329.1:c.6344-214_6344-212delinsCTG	XP_016864818.1:n.6344-214_6344-212delinsCTG
XM_017009330.2:c.4727-214_4727-212delinsCTG	XP_016864819.1:n.4727-214_4727-212delinsCTG
XM_017009331.1:c.4718-214_4718-212delinsCTG	XP_016864820.1:n.4718-214_4718-212delinsCTG
NM_133433.4:c.6344-214_6344-212delinsCTG MANE Select	NP_597677.2:n.6344-214_6344-212delinsCTG
NM_015384.5:c.6344-214_6344-212delinsCTG	NP_056199.2:n.6344-214_6344-212delinsCTG