Canonical Allele Identifier: CA1551843468

Gene: CWC27

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.64885447G= , CM000667.2:g.64885447G=	GRCh38
NC_000005.9:g.64181274G= , CM000667.1:g.64181274G=	GRCh37
NC_000005.8:g.64217030G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005869.4:c.943G= MANE Select	NP_005860.2:p.Glu315=
ENST00000381070.8:c.943G= MANE Select	ENSP00000370460.2:p.Glu315=
NM_001297644.1:c.943G=	NP_001284573.1:p.Glu315=
NM_001364478.1:c.943G=	NP_001351407.1:p.Glu315=
NM_005869.3:c.943G=	NP_005860.2:p.Glu315=
ENST00000381070.7:c.943G=	ENSP00000370460.2:p.Glu315=
ENST00000545000.1:n.135G=
ENST00000545000.2:n.135G=
ENST00000607786.2:c.643G=	ENSP00000509647.1:p.Glu215=
ENST00000687101.1:n.4059G=
ENST00000687314.1:c.943G=	ENSP00000510578.1:p.Glu315=
ENST00000688318.1:c.943G=	ENSP00000508653.1:p.Glu315=
ENST00000689534.1:n.1144G=
ENST00000691921.1:c.943G=	ENSP00000509657.1:p.Glu315=
ENST00000692005.1:c.844G=	ENSP00000509199.1:p.Glu282=
ENST00000692572.1:n.57G=
ENST00000692763.1:c.943G=	ENSP00000510726.1:p.Glu315=
ENST00000693121.1:n.4040G=
ENST00000693303.1:c.943G=	ENSP00000508557.1:p.Glu315=
ENST00000693660.1:c.844G=	ENSP00000509052.1:p.Glu282=
XM_011543095.1:c.943G=	XP_011541397.1:p.Glu315=
XM_011543095.3:c.943G=	XP_011541397.2:p.Glu315=