Canonical Allele Identifier: CA2716008

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180651431A>G , CM000665.2:g.180651431A>G	GRCh38
NC_000003.11:g.180369219A>G , CM000665.1:g.180369219A>G	GRCh37
NC_000003.10:g.181851913A>G	NCBI36
NG_029581.1:g.33065T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.1137T>C MANE Select	NP_852091.1:p.Asp379=
ENST00000476379.6:c.1137T>C MANE Select	ENSP00000417960.2:p.Asp379=
NM_181426.1:c.1137T>C	NP_852091.1:p.Asp379=
ENST00000442201.6:c.1137T>C	ENSP00000405708.2:p.Asp379=
ENST00000476379.5:c.1137T>C	ENSP00000417960.1:p.Asp379=
ENST00000650641.1:n.1024T>C
ENST00000650889.1:n.1528T>C
ENST00000651046.1:c.945T>C	ENSP00000499175.1:p.Asp315=
ENST00000651818.1:n.1087T>C
ENST00000651922.1:n.462T>C
ENST00000652024.1:n.1036T>C
ENST00000652408.1:n.1274T>C