Canonical Allele Identifier: CA355309847

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180644259T>C , CM000665.2:g.180644259T>C	GRCh38
NC_000003.11:g.180362047T>C , CM000665.1:g.180362047T>C	GRCh37
NC_000003.10:g.181844741T>C	NCBI36
NG_029581.1:g.40237A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.1528-2A>G MANE Select	NP_852091.1:n.1528-2A>G
ENST00000476379.6:c.1528-2A>G MANE Select	ENSP00000417960.2:n.1528-2A>G
NM_181426.1:c.1528-2A>G	NP_852091.1:n.1528-2A>G
ENST00000442201.6:c.1528-2A>G	ENSP00000405708.2:n.1528-2A>G
ENST00000476379.5:c.1528-2A>G	ENSP00000417960.1:n.1528-2A>G
ENST00000650641.1:n.1415-2A>G
ENST00000650889.1:n.4738A>G
ENST00000651046.1:c.1336-2A>G	ENSP00000499175.1:n.1336-2A>G
ENST00000651818.1:n.1478-2A>G
ENST00000651922.1:n.853-2A>G
ENST00000652024.1:n.4246A>G
ENST00000652408.1:n.1665-2A>G