Canonical Allele Identifier: CA2830535992

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180644292T>A , CM000665.2:g.180644292T>A	GRCh38
NC_000003.11:g.180362080T>A , CM000665.1:g.180362080T>A	GRCh37
NC_000003.10:g.181844774T>A	NCBI36
NG_029581.1:g.40204A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.1528-35A>T MANE Select	ENSP00000417960.2:n.1528-35A>T
ENST00000650641.1:n.1415-35A>T
ENST00000650889.1:n.4705A>T
ENST00000651046.1:c.1336-35A>T	ENSP00000499175.1:n.1336-35A>T
ENST00000651818.1:n.1478-35A>T
ENST00000651922.1:n.853-35A>T
ENST00000652024.1:n.4213A>T
ENST00000652408.1:n.1665-35A>T
ENST00000442201.6:c.1528-35A>T	ENSP00000405708.2:n.1528-35A>T
ENST00000476379.5:c.1528-35A>T	ENSP00000417960.1:n.1528-35A>T
NM_181426.1:c.1528-35A>T	NP_852091.1:n.1528-35A>T
NM_181426.2:c.1528-35A>T MANE Select	NP_852091.1:n.1528-35A>T