Canonical Allele Identifier: CA1424319490

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180679284A>C , CM000665.2:g.180679284A>C	GRCh38
NC_000003.11:g.180397072A>C , CM000665.1:g.180397072A>C	GRCh37
NC_000003.10:g.181879766A>C	NCBI36
NG_029581.1:g.5212T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.90+7T>G MANE Select	NP_852091.1:n.90+7T>G
ENST00000476379.6:c.90+7T>G MANE Select	ENSP00000417960.2:n.90+7T>G
NM_181426.1:c.90+7T>G	NP_852091.1:n.90+7T>G
ENST00000442201.6:c.90+7T>G	ENSP00000405708.2:n.90+7T>G
ENST00000471307.6:c.37-15298T>G	ENSP00000418702.2:n.37-15298T>G
ENST00000476379.5:c.90+7T>G	ENSP00000417960.1:n.90+7T>G
ENST00000650641.1:n.169+7T>G
ENST00000650889.1:n.262+324T>G
ENST00000651046.1:c.90+7T>G	ENSP00000499175.1:n.90+7T>G
ENST00000651818.1:n.232+324T>G
ENST00000652024.1:n.181+7T>G
ENST00000652408.1:n.227+324T>G