Canonical Allele Identifier: CA444096508

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064772C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064670C>T , CM000667.2:g.37064670C>T	GRCh38
NC_000005.9:g.37064772C>T , CM000667.1:g.37064772C>T	GRCh37
NC_000005.8:g.37100529C>T	NCBI36
NG_006987.1:g.192788C>T
NG_006987.2:g.192788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8193C>T (NIPBL) MANE Select	ENSP00000282516.8:p.Thr2731=
ENST00000652901.1:c.*137C>T (NIPBL)	ENSP00000499536.1:n.*137C>T
ENST00000282516.12:c.8193C>T (NIPBL)	ENSP00000282516.8:p.Thr2731=
ENST00000514335.1:n.2116C>T (NIPBL)
ENST00000621733.1:c.93C>T (NIPBL)	ENSP00000480694.1:p.Thr31=
NM_015384.4:c.*647C>T (NIPBL)	NP_056199.2:n.*647C>T
NM_133433.3:c.8193C>T (NIPBL)	NP_597677.2:p.Thr2731=
XM_005248280.2:c.*137C>T (NIPBL)	XP_005248337.1:n.*137C>T
XM_005248282.3:c.7449C>T (NIPBL)	XP_005248339.2:p.Thr2483=
XM_006714467.2:c.8046C>T (NIPBL)	XP_006714530.1:p.Thr2682=
XM_006714468.1:c.7995C>T (NIPBL)	XP_006714531.1:p.Thr2665=
XM_011514014.1:c.7812C>T (NIPBL)	XP_011512316.1:p.Thr2604=
XM_005248280.3:c.*137C>T (NIPBL)	XP_005248337.1:n.*137C>T
XM_005248282.5:c.7533C>T (NIPBL)	XP_005248339.3:p.Thr2511=
XM_006714468.2:c.7995C>T (NIPBL)	XP_006714531.1:p.Thr2665=
XM_017009329.1:c.*137C>T (NIPBL)	XP_016864818.1:n.*137C>T
XM_017009330.2:c.6576C>T (NIPBL)	XP_016864819.1:p.Thr2192=
XM_017009331.1:c.6567C>T (NIPBL)	XP_016864820.1:p.Thr2189=
XR_925644.2:n.12012G>A (CPLANE1)
NM_133433.4:c.8193C>T (NIPBL) MANE Select	NP_597677.2:p.Thr2731=
NM_015384.5:c.*647C>T (NIPBL)	NP_056199.2:n.*647C>T