Canonical Allele Identifier: CA2673577242

Gene: NIPBL CPLANE1

Linked Data

• gnomAD v4: 5-37064410-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064410G>A , CM000667.2:g.37064410G>A	GRCh38
NC_000005.9:g.37064512G>A , CM000667.1:g.37064512G>A	GRCh37
NC_000005.8:g.37100269G>A	NCBI36
NG_006987.1:g.192528G>A
NG_006987.2:g.192528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8050-117G>A (NIPBL) MANE Select	ENSP00000282516.8:n.8050-117G>A
ENST00000652901.1:c.7944-117G>A (NIPBL)	ENSP00000499536.1:n.7944-117G>A
ENST00000282516.12:c.8050-117G>A (NIPBL)	ENSP00000282516.8:n.8050-117G>A
ENST00000514335.1:n.1973-117G>A (NIPBL)
ENST00000621733.1:c.1-168G>A (NIPBL)	ENSP00000480694.1:n.1-168G>A
NM_015384.4:c.*387G>A (NIPBL)	NP_056199.2:n.*387G>A
NM_133433.3:c.8050-117G>A (NIPBL)	NP_597677.2:n.8050-117G>A
XM_005248280.2:c.8091-117G>A (NIPBL)	XP_005248337.1:n.8091-117G>A
XM_005248282.3:c.7306-117G>A (NIPBL)	XP_005248339.2:n.7306-117G>A
XM_006714467.2:c.7903-117G>A (NIPBL)	XP_006714530.1:n.7903-117G>A
XM_006714468.1:c.7852-117G>A (NIPBL)	XP_006714531.1:n.7852-117G>A
XM_011514014.1:c.7669-117G>A (NIPBL)	XP_011512316.1:n.7669-117G>A
XM_005248280.3:c.8091-117G>A (NIPBL)	XP_005248337.1:n.8091-117G>A
XM_005248282.5:c.7390-117G>A (NIPBL)	XP_005248339.3:n.7390-117G>A
XM_006714468.2:c.7852-117G>A (NIPBL)	XP_006714531.1:n.7852-117G>A
XM_017009329.1:c.7944-117G>A (NIPBL)	XP_016864818.1:n.7944-117G>A
XM_017009330.2:c.6433-117G>A (NIPBL)	XP_016864819.1:n.6433-117G>A
XM_017009331.1:c.6424-117G>A (NIPBL)	XP_016864820.1:n.6424-117G>A
XR_925644.2:n.12272C>T (CPLANE1)
NM_133433.4:c.8050-117G>A (NIPBL) MANE Select	NP_597677.2:n.8050-117G>A
NM_015384.5:c.*387G>A (NIPBL)	NP_056199.2:n.*387G>A