Canonical Allele Identifier: CA355301853

Gene: CCDC39

Linked Data

• MyVariant Identifiers: chr3:g.180377244G>A (hg19) ; chr3:g.180659456G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659456G>A , CM000665.2:g.180659456G>A	GRCh38
NC_000003.11:g.180377244G>A , CM000665.1:g.180377244G>A	GRCh37
NC_000003.10:g.181859938G>A	NCBI36
NG_029581.1:g.25040C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.734C>T MANE Select	ENSP00000417960.2:p.Ala245Val
ENST00000650641.1:n.813C>T
ENST00000650889.1:n.906C>T
ENST00000651046.1:c.734C>T	ENSP00000499175.1:p.Ala245Val
ENST00000651818.1:n.876C>T
ENST00000652024.1:n.825C>T
ENST00000652408.1:n.871C>T
ENST00000442201.6:c.734C>T	ENSP00000405708.2:p.Ala245Val
ENST00000476379.5:c.734C>T	ENSP00000417960.1:p.Ala245Val
NM_181426.1:c.734C>T	NP_852091.1:p.Ala245Val
NM_181426.2:c.734C>T MANE Select	NP_852091.1:p.Ala245Val