Canonical Allele Identifier: CA359522482

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064770A>G (hg19) ; chr5:g.37064668A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064668A>G , CM000667.2:g.37064668A>G	GRCh38
NC_000005.9:g.37064770A>G , CM000667.1:g.37064770A>G	GRCh37
NC_000005.8:g.37100527A>G	NCBI36
NG_006987.1:g.192786A>G
NG_006987.2:g.192786A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8191A>G (NIPBL) MANE Select	ENSP00000282516.8:p.Thr2731Ala
ENST00000652901.1:c.*135A>G (NIPBL)	ENSP00000499536.1:n.*135A>G
ENST00000282516.12:c.8191A>G (NIPBL)	ENSP00000282516.8:p.Thr2731Ala
ENST00000514335.1:n.2114A>G (NIPBL)
ENST00000621733.1:c.91A>G (NIPBL)	ENSP00000480694.1:p.Thr31Ala
NM_015384.4:c.*645A>G (NIPBL)	NP_056199.2:n.*645A>G
NM_133433.3:c.8191A>G (NIPBL)	NP_597677.2:p.Thr2731Ala
XM_005248280.2:c.*135A>G (NIPBL)	XP_005248337.1:n.*135A>G
XM_005248282.3:c.7447A>G (NIPBL)	XP_005248339.2:p.Thr2483Ala
XM_006714467.2:c.8044A>G (NIPBL)	XP_006714530.1:p.Thr2682Ala
XM_006714468.1:c.7993A>G (NIPBL)	XP_006714531.1:p.Thr2665Ala
XM_011514014.1:c.7810A>G (NIPBL)	XP_011512316.1:p.Thr2604Ala
XM_005248280.3:c.*135A>G (NIPBL)	XP_005248337.1:n.*135A>G
XM_005248282.5:c.7531A>G (NIPBL)	XP_005248339.3:p.Thr2511Ala
XM_006714468.2:c.7993A>G (NIPBL)	XP_006714531.1:p.Thr2665Ala
XM_017009329.1:c.*135A>G (NIPBL)	XP_016864818.1:n.*135A>G
XM_017009330.2:c.6574A>G (NIPBL)	XP_016864819.1:p.Thr2192Ala
XM_017009331.1:c.6565A>G (NIPBL)	XP_016864820.1:p.Thr2189Ala
XR_925644.2:n.12014T>C (CPLANE1)
NM_133433.4:c.8191A>G (NIPBL) MANE Select	NP_597677.2:p.Thr2731Ala
NM_015384.5:c.*645A>G (NIPBL)	NP_056199.2:n.*645A>G