Canonical Allele Identifier: CA359522519

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064782T>A (hg19) ; chr5:g.37064680T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064680T>A , CM000667.2:g.37064680T>A	GRCh38
NC_000005.9:g.37064782T>A , CM000667.1:g.37064782T>A	GRCh37
NC_000005.8:g.37100539T>A	NCBI36
NG_006987.1:g.192798T>A
NG_006987.2:g.192798T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8203T>A (NIPBL) MANE Select	ENSP00000282516.8:p.Phe2735Ile
ENST00000652901.1:c.*147T>A (NIPBL)	ENSP00000499536.1:n.*147T>A
ENST00000282516.12:c.8203T>A (NIPBL)	ENSP00000282516.8:p.Phe2735Ile
ENST00000514335.1:n.2126T>A (NIPBL)
ENST00000621733.1:c.103T>A (NIPBL)	ENSP00000480694.1:p.Phe35Ile
NM_015384.4:c.*657T>A (NIPBL)	NP_056199.2:n.*657T>A
NM_133433.3:c.8203T>A (NIPBL)	NP_597677.2:p.Phe2735Ile
XM_005248280.2:c.*147T>A (NIPBL)	XP_005248337.1:n.*147T>A
XM_005248282.3:c.7459T>A (NIPBL)	XP_005248339.2:p.Phe2487Ile
XM_006714467.2:c.8056T>A (NIPBL)	XP_006714530.1:p.Phe2686Ile
XM_006714468.1:c.8005T>A (NIPBL)	XP_006714531.1:p.Phe2669Ile
XM_011514014.1:c.7822T>A (NIPBL)	XP_011512316.1:p.Phe2608Ile
XM_005248280.3:c.*147T>A (NIPBL)	XP_005248337.1:n.*147T>A
XM_005248282.5:c.7543T>A (NIPBL)	XP_005248339.3:p.Phe2515Ile
XM_006714468.2:c.8005T>A (NIPBL)	XP_006714531.1:p.Phe2669Ile
XM_017009329.1:c.*147T>A (NIPBL)	XP_016864818.1:n.*147T>A
XM_017009330.2:c.6586T>A (NIPBL)	XP_016864819.1:p.Phe2196Ile
XM_017009331.1:c.6577T>A (NIPBL)	XP_016864820.1:p.Phe2193Ile
XR_925644.2:n.12002A>T (CPLANE1)
NM_133433.4:c.8203T>A (NIPBL) MANE Select	NP_597677.2:p.Phe2735Ile
NM_015384.5:c.*657T>A (NIPBL)	NP_056199.2:n.*657T>A