Canonical Allele Identifier: CA437080180

Gene: CCDC39

Linked Data

• MyVariant Identifiers: chr3:g.180377243A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659455A>T , CM000665.2:g.180659455A>T	GRCh38
NC_000003.11:g.180377243A>T , CM000665.1:g.180377243A>T	GRCh37
NC_000003.10:g.181859937A>T	NCBI36
NG_029581.1:g.25041T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.735T>A MANE Select	ENSP00000417960.2:p.Ala245=
ENST00000650641.1:n.814T>A
ENST00000650889.1:n.907T>A
ENST00000651046.1:c.735T>A	ENSP00000499175.1:p.Ala245=
ENST00000651818.1:n.877T>A
ENST00000652024.1:n.826T>A
ENST00000652408.1:n.872T>A
ENST00000442201.6:c.735T>A	ENSP00000405708.2:p.Ala245=
ENST00000476379.5:c.735T>A	ENSP00000417960.1:p.Ala245=
NM_181426.1:c.735T>A	NP_852091.1:p.Ala245=
NM_181426.2:c.735T>A MANE Select	NP_852091.1:p.Ala245=