Canonical Allele Identifier: CA359523917

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064978A>T (hg19) ; chr5:g.37064876A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064876A>T , CM000667.2:g.37064876A>T	GRCh38
NC_000005.9:g.37064978A>T , CM000667.1:g.37064978A>T	GRCh37
NC_000005.8:g.37100735A>T	NCBI36
NG_006987.1:g.192994A>T
NG_006987.2:g.192994A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.8399A>T (NIPBL) MANE Select	ENSP00000282516.8:p.Asp2800Val
ENST00000652901.1:c.*343A>T (NIPBL)	ENSP00000499536.1:n.*343A>T
ENST00000282516.12:c.8399A>T (NIPBL)	ENSP00000282516.8:p.Asp2800Val
ENST00000514335.1:n.2322A>T (NIPBL)
ENST00000621733.1:c.299A>T (NIPBL)	ENSP00000480694.1:p.Asp100Val
NM_015384.4:c.*853A>T (NIPBL)	NP_056199.2:n.*853A>T
NM_133433.3:c.8399A>T (NIPBL)	NP_597677.2:p.Asp2800Val
XM_005248280.2:c.*343A>T (NIPBL)	XP_005248337.1:n.*343A>T
XM_005248282.3:c.7655A>T (NIPBL)	XP_005248339.2:p.Asp2552Val
XM_006714467.2:c.8252A>T (NIPBL)	XP_006714530.1:p.Asp2751Val
XM_006714468.1:c.8201A>T (NIPBL)	XP_006714531.1:p.Asp2734Val
XM_011514014.1:c.8018A>T (NIPBL)	XP_011512316.1:p.Asp2673Val
XM_005248280.3:c.*343A>T (NIPBL)	XP_005248337.1:n.*343A>T
XM_005248282.5:c.7739A>T (NIPBL)	XP_005248339.3:p.Asp2580Val
XM_006714468.2:c.8201A>T (NIPBL)	XP_006714531.1:p.Asp2734Val
XM_017009329.1:c.*343A>T (NIPBL)	XP_016864818.1:n.*343A>T
XM_017009330.2:c.6782A>T (NIPBL)	XP_016864819.1:p.Asp2261Val
XM_017009331.1:c.6773A>T (NIPBL)	XP_016864820.1:p.Asp2258Val
XR_925644.2:n.11806T>A (CPLANE1)
NM_133433.4:c.8399A>T (NIPBL) MANE Select	NP_597677.2:p.Asp2800Val
NM_015384.5:c.*853A>T (NIPBL)	NP_056199.2:n.*853A>T