Canonical Allele Identifier: CA444096492

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064754A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064652A>T , CM000667.2:g.37064652A>T	GRCh38
NC_000005.9:g.37064754A>T , CM000667.1:g.37064754A>T	GRCh37
NC_000005.8:g.37100511A>T	NCBI36
NG_006987.1:g.192770A>T
NG_006987.2:g.192770A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8175A>T (NIPBL) MANE Select	ENSP00000282516.8:p.Ala2725=
ENST00000652901.1:c.*119A>T (NIPBL)	ENSP00000499536.1:n.*119A>T
ENST00000282516.12:c.8175A>T (NIPBL)	ENSP00000282516.8:p.Ala2725=
ENST00000514335.1:n.2098A>T (NIPBL)
ENST00000621733.1:c.75A>T (NIPBL)	ENSP00000480694.1:p.Ala25=
NM_015384.4:c.*629A>T (NIPBL)	NP_056199.2:n.*629A>T
NM_133433.3:c.8175A>T (NIPBL)	NP_597677.2:p.Ala2725=
XM_005248280.2:c.*119A>T (NIPBL)	XP_005248337.1:n.*119A>T
XM_005248282.3:c.7431A>T (NIPBL)	XP_005248339.2:p.Ala2477=
XM_006714467.2:c.8028A>T (NIPBL)	XP_006714530.1:p.Ala2676=
XM_006714468.1:c.7977A>T (NIPBL)	XP_006714531.1:p.Ala2659=
XM_011514014.1:c.7794A>T (NIPBL)	XP_011512316.1:p.Ala2598=
XM_005248280.3:c.*119A>T (NIPBL)	XP_005248337.1:n.*119A>T
XM_005248282.5:c.7515A>T (NIPBL)	XP_005248339.3:p.Ala2505=
XM_006714468.2:c.7977A>T (NIPBL)	XP_006714531.1:p.Ala2659=
XM_017009329.1:c.*119A>T (NIPBL)	XP_016864818.1:n.*119A>T
XM_017009330.2:c.6558A>T (NIPBL)	XP_016864819.1:p.Ala2186=
XM_017009331.1:c.6549A>T (NIPBL)	XP_016864820.1:p.Ala2183=
XR_925644.2:n.12030T>A (CPLANE1)
NM_133433.4:c.8175A>T (NIPBL) MANE Select	NP_597677.2:p.Ala2725=
NM_015384.5:c.*629A>T (NIPBL)	NP_056199.2:n.*629A>T