Canonical Allele Identifier: CA2765908573

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36876791C>G , CM000667.2:g.36876791C>G	GRCh38
NC_000005.9:g.36876893C>G , CM000667.1:g.36876893C>G	GRCh37
NC_000005.8:g.36912650C>G	NCBI36
NG_006987.1:g.4909C>G
NG_006987.2:g.4909C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.-467C>G MANE Select	ENSP00000282516.8:n.-467C>G
ENST00000282516.12:c.-467C>G	ENSP00000282516.8:n.-467C>G
ENST00000448238.2:c.-467C>G	ENSP00000406266.2:n.-467C>G
NM_015384.4:c.-467C>G	NP_056199.2:n.-467C>G
NM_133433.3:c.-467C>G	NP_597677.2:n.-467C>G
XM_005248280.2:c.-467C>G	XP_005248337.1:n.-467C>G
XM_006714467.2:c.-467C>G	XP_006714530.1:n.-467C>G
XM_006714468.1:c.-467C>G	XP_006714531.1:n.-467C>G
XM_011514014.1:c.-467C>G	XP_011512316.1:n.-467C>G
XM_011514015.1:c.-467C>G	XP_011512317.1:n.-467C>G
XM_005248280.3:c.-467C>G	XP_005248337.1:n.-467C>G
XM_006714468.2:c.-467C>G	XP_006714531.1:n.-467C>G
XM_017009329.1:c.-467C>G	XP_016864818.1:n.-467C>G
XM_017009331.1:c.-467C>G	XP_016864820.1:n.-467C>G
NM_133433.4:c.-467C>G MANE Select	NP_597677.2:n.-467C>G
NM_015384.5:c.-467C>G	NP_056199.2:n.-467C>G