Canonical Allele Identifier: CA359522515

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064780G>T (hg19) ; chr5:g.37064678G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064678G>T , CM000667.2:g.37064678G>T	GRCh38
NC_000005.9:g.37064780G>T , CM000667.1:g.37064780G>T	GRCh37
NC_000005.8:g.37100537G>T	NCBI36
NG_006987.1:g.192796G>T
NG_006987.2:g.192796G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8201G>T (NIPBL) MANE Select	ENSP00000282516.8:p.Gly2734Val
ENST00000652901.1:c.*145G>T (NIPBL)	ENSP00000499536.1:n.*145G>T
ENST00000282516.12:c.8201G>T (NIPBL)	ENSP00000282516.8:p.Gly2734Val
ENST00000514335.1:n.2124G>T (NIPBL)
ENST00000621733.1:c.101G>T (NIPBL)	ENSP00000480694.1:p.Gly34Val
NM_015384.4:c.*655G>T (NIPBL)	NP_056199.2:n.*655G>T
NM_133433.3:c.8201G>T (NIPBL)	NP_597677.2:p.Gly2734Val
XM_005248280.2:c.*145G>T (NIPBL)	XP_005248337.1:n.*145G>T
XM_005248282.3:c.7457G>T (NIPBL)	XP_005248339.2:p.Gly2486Val
XM_006714467.2:c.8054G>T (NIPBL)	XP_006714530.1:p.Gly2685Val
XM_006714468.1:c.8003G>T (NIPBL)	XP_006714531.1:p.Gly2668Val
XM_011514014.1:c.7820G>T (NIPBL)	XP_011512316.1:p.Gly2607Val
XM_005248280.3:c.*145G>T (NIPBL)	XP_005248337.1:n.*145G>T
XM_005248282.5:c.7541G>T (NIPBL)	XP_005248339.3:p.Gly2514Val
XM_006714468.2:c.8003G>T (NIPBL)	XP_006714531.1:p.Gly2668Val
XM_017009329.1:c.*145G>T (NIPBL)	XP_016864818.1:n.*145G>T
XM_017009330.2:c.6584G>T (NIPBL)	XP_016864819.1:p.Gly2195Val
XM_017009331.1:c.6575G>T (NIPBL)	XP_016864820.1:p.Gly2192Val
XR_925644.2:n.12004C>A (CPLANE1)
NM_133433.4:c.8201G>T (NIPBL) MANE Select	NP_597677.2:p.Gly2734Val
NM_015384.5:c.*655G>T (NIPBL)	NP_056199.2:n.*655G>T