Canonical Allele Identifier: CA437080227

Gene: CCDC39

Linked Data

• MyVariant Identifiers: chr3:g.180377348T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659560T>G , CM000665.2:g.180659560T>G	GRCh38
NC_000003.11:g.180377348T>G , CM000665.1:g.180377348T>G	GRCh37
NC_000003.10:g.181860042T>G	NCBI36
NG_029581.1:g.24936A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.630A>C MANE Select	ENSP00000417960.2:p.Ala210=
ENST00000650641.1:n.709A>C
ENST00000650889.1:n.802A>C
ENST00000651046.1:c.630A>C	ENSP00000499175.1:p.Ala210=
ENST00000651818.1:n.772A>C
ENST00000652024.1:n.721A>C
ENST00000652408.1:n.767A>C
ENST00000442201.6:c.630A>C	ENSP00000405708.2:p.Ala210=
ENST00000476379.5:c.630A>C	ENSP00000417960.1:p.Ala210=
NM_181426.1:c.630A>C	NP_852091.1:p.Ala210=
NM_181426.2:c.630A>C MANE Select	NP_852091.1:p.Ala210=