Canonical Allele Identifier: CA1424310364

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659493G= , CM000665.2:g.180659493G=	GRCh38
NC_000003.11:g.180377281G= , CM000665.1:g.180377281G=	GRCh37
NC_000003.10:g.181859975G=	NCBI36
NG_029581.1:g.25003C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.697C= MANE Select	ENSP00000417960.2:p.Gln233=
ENST00000650641.1:n.776C=
ENST00000650889.1:n.869C=
ENST00000651046.1:c.697C=	ENSP00000499175.1:p.Gln233=
ENST00000651818.1:n.839C=
ENST00000652024.1:n.788C=
ENST00000652408.1:n.834C=
ENST00000442201.6:c.697C=	ENSP00000405708.2:p.Gln233=
ENST00000476379.5:c.697C=	ENSP00000417960.1:p.Gln233=
NM_181426.1:c.697C=	NP_852091.1:p.Gln233=
NM_181426.2:c.697C= MANE Select	NP_852091.1:p.Gln233=