Canonical Allele Identifier: CA2577967089

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659667T>C , CM000665.2:g.180659667T>C	GRCh38
NC_000003.11:g.180377455T>C , CM000665.1:g.180377455T>C	GRCh37
NC_000003.10:g.181860149T>C	NCBI36
NG_029581.1:g.24829A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.609+10A>G MANE Select	ENSP00000417960.2:n.609+10A>G
ENST00000650641.1:n.688+10A>G
ENST00000650889.1:n.781+10A>G
ENST00000651046.1:c.609+10A>G	ENSP00000499175.1:n.609+10A>G
ENST00000651818.1:n.751+10A>G
ENST00000652024.1:n.700+10A>G
ENST00000652408.1:n.746+10A>G
ENST00000442201.6:c.609+10A>G	ENSP00000405708.2:n.609+10A>G
ENST00000476379.5:c.609+10A>G	ENSP00000417960.1:n.609+10A>G
NM_181426.1:c.609+10A>G	NP_852091.1:n.609+10A>G
NM_181426.2:c.609+10A>G MANE Select	NP_852091.1:n.609+10A>G