Canonical Allele Identifier: CA437080250

Gene: CCDC39

Linked Data

• MyVariant Identifiers: chr3:g.180377468T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659680T>G , CM000665.2:g.180659680T>G	GRCh38
NC_000003.11:g.180377468T>G , CM000665.1:g.180377468T>G	GRCh37
NC_000003.10:g.181860162T>G	NCBI36
NG_029581.1:g.24816A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000476379.6:c.606A>C MANE Select	ENSP00000417960.2:p.Ala202=
ENST00000650641.1:n.685A>C
ENST00000650889.1:n.778A>C
ENST00000651046.1:c.606A>C	ENSP00000499175.1:p.Ala202=
ENST00000651818.1:n.748A>C
ENST00000652024.1:n.697A>C
ENST00000652408.1:n.743A>C
ENST00000442201.6:c.606A>C	ENSP00000405708.2:p.Ala202=
ENST00000476379.5:c.606A>C	ENSP00000417960.1:p.Ala202=
NM_181426.1:c.606A>C	NP_852091.1:p.Ala202=
NM_181426.2:c.606A>C MANE Select	NP_852091.1:p.Ala202=