Canonical Allele Identifier: CA355301950

Gene: CCDC39

Linked Data

• MyVariant Identifiers: chr3:g.180377265T>A (hg19) ; chr3:g.180659477T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659477T>A , CM000665.2:g.180659477T>A	GRCh38
NC_000003.11:g.180377265T>A , CM000665.1:g.180377265T>A	GRCh37
NC_000003.10:g.181859959T>A	NCBI36
NG_029581.1:g.25019A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.713A>T MANE Select	ENSP00000417960.2:p.Asp238Val
ENST00000650641.1:n.792A>T
ENST00000650889.1:n.885A>T
ENST00000651046.1:c.713A>T	ENSP00000499175.1:p.Asp238Val
ENST00000651818.1:n.855A>T
ENST00000652024.1:n.804A>T
ENST00000652408.1:n.850A>T
ENST00000442201.6:c.713A>T	ENSP00000405708.2:p.Asp238Val
ENST00000476379.5:c.713A>T	ENSP00000417960.1:p.Asp238Val
NM_181426.1:c.713A>T	NP_852091.1:p.Asp238Val
NM_181426.2:c.713A>T MANE Select	NP_852091.1:p.Asp238Val