Canonical Allele Identifier: CA2673554299

Gene: NIPBL

Linked Data

• gnomAD v4: 5-37010239-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37010239T>A , CM000667.2:g.37010239T>A	GRCh38
NC_000005.9:g.37010341T>A , CM000667.1:g.37010341T>A	GRCh37
NC_000005.8:g.37046098T>A	NCBI36
NG_006987.1:g.138357T>A
NG_006987.2:g.138357T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4560+14T>A MANE Select	ENSP00000282516.8:n.4560+14T>A
ENST00000652901.1:c.4560+14T>A	ENSP00000499536.1:n.4560+14T>A
ENST00000282516.12:c.4560+14T>A	ENSP00000282516.8:n.4560+14T>A
ENST00000448238.2:c.4560+14T>A	ENSP00000406266.2:n.4560+14T>A
ENST00000621733.1:c.1-54339T>A	ENSP00000480694.1:n.1-54339T>A
NM_015384.4:c.4560+14T>A	NP_056199.2:n.4560+14T>A
NM_133433.3:c.4560+14T>A	NP_597677.2:n.4560+14T>A
XM_005248280.2:c.4560+14T>A	XP_005248337.1:n.4560+14T>A
XM_005248282.3:c.3816+14T>A	XP_005248339.2:n.3816+14T>A
XM_006714467.2:c.4560+14T>A	XP_006714530.1:n.4560+14T>A
XM_006714468.1:c.4362+14T>A	XP_006714531.1:n.4362+14T>A
XM_011514014.1:c.4179+14T>A	XP_011512316.1:n.4179+14T>A
XM_011514015.1:c.4560+14T>A	XP_011512317.1:n.4560+14T>A
XM_005248280.3:c.4560+14T>A	XP_005248337.1:n.4560+14T>A
XM_005248282.5:c.3900+14T>A	XP_005248339.3:n.3900+14T>A
XM_006714468.2:c.4362+14T>A	XP_006714531.1:n.4362+14T>A
XM_017009329.1:c.4560+14T>A	XP_016864818.1:n.4560+14T>A
XM_017009330.2:c.2943+14T>A	XP_016864819.1:n.2943+14T>A
XM_017009331.1:c.2934+14T>A	XP_016864820.1:n.2934+14T>A
NM_133433.4:c.4560+14T>A MANE Select	NP_597677.2:n.4560+14T>A
NM_015384.5:c.4560+14T>A	NP_056199.2:n.4560+14T>A