Canonical Allele Identifier: CA1424310344

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659462T= , CM000665.2:g.180659462T=	GRCh38
NC_000003.11:g.180377250T= , CM000665.1:g.180377250T=	GRCh37
NC_000003.10:g.181859944T=	NCBI36
NG_029581.1:g.25034A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.728A= MANE Select	ENSP00000417960.2:p.Asn243=
ENST00000650641.1:n.807A=
ENST00000650889.1:n.900A=
ENST00000651046.1:c.728A=	ENSP00000499175.1:p.Asn243=
ENST00000651818.1:n.870A=
ENST00000652024.1:n.819A=
ENST00000652408.1:n.865A=
ENST00000442201.6:c.728A=	ENSP00000405708.2:p.Asn243=
ENST00000476379.5:c.728A=	ENSP00000417960.1:p.Asn243=
NM_181426.1:c.728A=	NP_852091.1:p.Asn243=
NM_181426.2:c.728A= MANE Select	NP_852091.1:p.Asn243=