Canonical Allele Identifier: CA355302084
Gene: CCDC39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659505T>G , CM000665.2:g.180659505T>G GRCh38
NC_000003.11:g.180377293T>G , CM000665.1:g.180377293T>G GRCh37
NC_000003.10:g.181859987T>G NCBI36
NG_029581.1:g.24991A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.685A>C MANE Select ENSP00000417960.2:p.Asn229His
ENST00000650641.1:n.764A>C
ENST00000650889.1:n.857A>C
ENST00000651046.1:c.685A>C ENSP00000499175.1:p.Asn229His
ENST00000651818.1:n.827A>C
ENST00000652024.1:n.776A>C
ENST00000652408.1:n.822A>C
ENST00000442201.6:c.685A>C ENSP00000405708.2:p.Asn229His
ENST00000476379.5:c.685A>C ENSP00000417960.1:p.Asn229His
NM_181426.1:c.685A>C NP_852091.1:p.Asn229His
NM_181426.2:c.685A>C MANE Select NP_852091.1:p.Asn229His