Canonical Allele Identifier: CA359522461

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064766G>T (hg19) ; chr5:g.37064664G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064664G>T , CM000667.2:g.37064664G>T	GRCh38
NC_000005.9:g.37064766G>T , CM000667.1:g.37064766G>T	GRCh37
NC_000005.8:g.37100523G>T	NCBI36
NG_006987.1:g.192782G>T
NG_006987.2:g.192782G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8187G>T (NIPBL) MANE Select	ENSP00000282516.8:p.Gln2729His
ENST00000652901.1:c.*131G>T (NIPBL)	ENSP00000499536.1:n.*131G>T
ENST00000282516.12:c.8187G>T (NIPBL)	ENSP00000282516.8:p.Gln2729His
ENST00000514335.1:n.2110G>T (NIPBL)
ENST00000621733.1:c.87G>T (NIPBL)	ENSP00000480694.1:p.Gln29His
NM_015384.4:c.*641G>T (NIPBL)	NP_056199.2:n.*641G>T
NM_133433.3:c.8187G>T (NIPBL)	NP_597677.2:p.Gln2729His
XM_005248280.2:c.*131G>T (NIPBL)	XP_005248337.1:n.*131G>T
XM_005248282.3:c.7443G>T (NIPBL)	XP_005248339.2:p.Gln2481His
XM_006714467.2:c.8040G>T (NIPBL)	XP_006714530.1:p.Gln2680His
XM_006714468.1:c.7989G>T (NIPBL)	XP_006714531.1:p.Gln2663His
XM_011514014.1:c.7806G>T (NIPBL)	XP_011512316.1:p.Gln2602His
XM_005248280.3:c.*131G>T (NIPBL)	XP_005248337.1:n.*131G>T
XM_005248282.5:c.7527G>T (NIPBL)	XP_005248339.3:p.Gln2509His
XM_006714468.2:c.7989G>T (NIPBL)	XP_006714531.1:p.Gln2663His
XM_017009329.1:c.*131G>T (NIPBL)	XP_016864818.1:n.*131G>T
XM_017009330.2:c.6570G>T (NIPBL)	XP_016864819.1:p.Gln2190His
XM_017009331.1:c.6561G>T (NIPBL)	XP_016864820.1:p.Gln2187His
XR_925644.2:n.12018C>A (CPLANE1)
NM_133433.4:c.8187G>T (NIPBL) MANE Select	NP_597677.2:p.Gln2729His
NM_015384.5:c.*641G>T (NIPBL)	NP_056199.2:n.*641G>T