Canonical Allele Identifier: CA359522587

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064797A>G (hg19) ; chr5:g.37064695A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064695A>G , CM000667.2:g.37064695A>G	GRCh38
NC_000005.9:g.37064797A>G , CM000667.1:g.37064797A>G	GRCh37
NC_000005.8:g.37100554A>G	NCBI36
NG_006987.1:g.192813A>G
NG_006987.2:g.192813A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8218A>G (NIPBL) MANE Select	ENSP00000282516.8:p.Met2740Val
ENST00000652901.1:c.*162A>G (NIPBL)	ENSP00000499536.1:n.*162A>G
ENST00000282516.12:c.8218A>G (NIPBL)	ENSP00000282516.8:p.Met2740Val
ENST00000514335.1:n.2141A>G (NIPBL)
ENST00000621733.1:c.118A>G (NIPBL)	ENSP00000480694.1:p.Met40Val
NM_015384.4:c.*672A>G (NIPBL)	NP_056199.2:n.*672A>G
NM_133433.3:c.8218A>G (NIPBL)	NP_597677.2:p.Met2740Val
XM_005248280.2:c.*162A>G (NIPBL)	XP_005248337.1:n.*162A>G
XM_005248282.3:c.7474A>G (NIPBL)	XP_005248339.2:p.Met2492Val
XM_006714467.2:c.8071A>G (NIPBL)	XP_006714530.1:p.Met2691Val
XM_006714468.1:c.8020A>G (NIPBL)	XP_006714531.1:p.Met2674Val
XM_011514014.1:c.7837A>G (NIPBL)	XP_011512316.1:p.Met2613Val
XM_005248280.3:c.*162A>G (NIPBL)	XP_005248337.1:n.*162A>G
XM_005248282.5:c.7558A>G (NIPBL)	XP_005248339.3:p.Met2520Val
XM_006714468.2:c.8020A>G (NIPBL)	XP_006714531.1:p.Met2674Val
XM_017009329.1:c.*162A>G (NIPBL)	XP_016864818.1:n.*162A>G
XM_017009330.2:c.6601A>G (NIPBL)	XP_016864819.1:p.Met2201Val
XM_017009331.1:c.6592A>G (NIPBL)	XP_016864820.1:p.Met2198Val
XR_925644.2:n.11987T>C (CPLANE1)
NM_133433.4:c.8218A>G (NIPBL) MANE Select	NP_597677.2:p.Met2740Val
NM_015384.5:c.*672A>G (NIPBL)	NP_056199.2:n.*672A>G