Canonical Allele Identifier: CA2716280

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180679379A>G , CM000665.2:g.180679379A>G	GRCh38
NC_000003.11:g.180397167A>G , CM000665.1:g.180397167A>G	GRCh37
NC_000003.10:g.181879861A>G	NCBI36
NG_029581.1:g.5117T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.2T>C MANE Select	NP_852091.1:p.Met1Thr
ENST00000476379.6:c.2T>C MANE Select	ENSP00000417960.2:p.Met1Thr
NM_181426.1:c.2T>C	NP_852091.1:p.Met1Thr
ENST00000442201.6:c.2T>C	ENSP00000405708.2:p.Met1Thr
ENST00000471307.6:c.37-15393T>C	ENSP00000418702.2:n.37-15393T>C
ENST00000476379.5:c.2T>C	ENSP00000417960.1:p.Met1Thr
ENST00000650641.1:n.81T>C
ENST00000650889.1:n.262+229T>C
ENST00000651046.1:c.2T>C	ENSP00000499175.1:p.Met1Thr
ENST00000651818.1:n.232+229T>C
ENST00000652024.1:n.93T>C
ENST00000652408.1:n.227+229T>C