Canonical Allele Identifier: CA1424310367

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659498A= , CM000665.2:g.180659498A=	GRCh38
NC_000003.11:g.180377286A= , CM000665.1:g.180377286A=	GRCh37
NC_000003.10:g.181859980A=	NCBI36
NG_029581.1:g.24998T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.692T= MANE Select	ENSP00000417960.2:p.Ile231=
ENST00000650641.1:n.771T=
ENST00000650889.1:n.864T=
ENST00000651046.1:c.692T=	ENSP00000499175.1:p.Ile231=
ENST00000651818.1:n.834T=
ENST00000652024.1:n.783T=
ENST00000652408.1:n.829T=
ENST00000442201.6:c.692T=	ENSP00000405708.2:p.Ile231=
ENST00000476379.5:c.692T=	ENSP00000417960.1:p.Ile231=
NM_181426.1:c.692T=	NP_852091.1:p.Ile231=
NM_181426.2:c.692T= MANE Select	NP_852091.1:p.Ile231=