Canonical Allele Identifier: CA359523798

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064966A>G (hg19) ; chr5:g.37064864A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064864A>G , CM000667.2:g.37064864A>G	GRCh38
NC_000005.9:g.37064966A>G , CM000667.1:g.37064966A>G	GRCh37
NC_000005.8:g.37100723A>G	NCBI36
NG_006987.1:g.192982A>G
NG_006987.2:g.192982A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.8387A>G (NIPBL) MANE Select	ENSP00000282516.8:p.Tyr2796Cys
ENST00000652901.1:c.*331A>G (NIPBL)	ENSP00000499536.1:n.*331A>G
ENST00000282516.12:c.8387A>G (NIPBL)	ENSP00000282516.8:p.Tyr2796Cys
ENST00000514335.1:n.2310A>G (NIPBL)
ENST00000621733.1:c.287A>G (NIPBL)	ENSP00000480694.1:p.Tyr96Cys
NM_015384.4:c.*841A>G (NIPBL)	NP_056199.2:n.*841A>G
NM_133433.3:c.8387A>G (NIPBL)	NP_597677.2:p.Tyr2796Cys
XM_005248280.2:c.*331A>G (NIPBL)	XP_005248337.1:n.*331A>G
XM_005248282.3:c.7643A>G (NIPBL)	XP_005248339.2:p.Tyr2548Cys
XM_006714467.2:c.8240A>G (NIPBL)	XP_006714530.1:p.Tyr2747Cys
XM_006714468.1:c.8189A>G (NIPBL)	XP_006714531.1:p.Tyr2730Cys
XM_011514014.1:c.8006A>G (NIPBL)	XP_011512316.1:p.Tyr2669Cys
XM_005248280.3:c.*331A>G (NIPBL)	XP_005248337.1:n.*331A>G
XM_005248282.5:c.7727A>G (NIPBL)	XP_005248339.3:p.Tyr2576Cys
XM_006714468.2:c.8189A>G (NIPBL)	XP_006714531.1:p.Tyr2730Cys
XM_017009329.1:c.*331A>G (NIPBL)	XP_016864818.1:n.*331A>G
XM_017009330.2:c.6770A>G (NIPBL)	XP_016864819.1:p.Tyr2257Cys
XM_017009331.1:c.6761A>G (NIPBL)	XP_016864820.1:p.Tyr2254Cys
XR_925644.2:n.11818T>C (CPLANE1)
NM_133433.4:c.8387A>G (NIPBL) MANE Select	NP_597677.2:p.Tyr2796Cys
NM_015384.5:c.*841A>G (NIPBL)	NP_056199.2:n.*841A>G