Canonical Allele Identifier: CA355301863
Gene: CCDC39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.180377246A>C (hg19) chr3:g.180659458A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659458A>C , CM000665.2:g.180659458A>C GRCh38
NC_000003.11:g.180377246A>C , CM000665.1:g.180377246A>C GRCh37
NC_000003.10:g.181859940A>C NCBI36
NG_029581.1:g.25038T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.732T>G MANE Select ENSP00000417960.2:p.Cys244Trp
ENST00000650641.1:n.811T>G
ENST00000650889.1:n.904T>G
ENST00000651046.1:c.732T>G ENSP00000499175.1:p.Cys244Trp
ENST00000651818.1:n.874T>G
ENST00000652024.1:n.823T>G
ENST00000652408.1:n.869T>G
ENST00000442201.6:c.732T>G ENSP00000405708.2:p.Cys244Trp
ENST00000476379.5:c.732T>G ENSP00000417960.1:p.Cys244Trp
NM_181426.1:c.732T>G NP_852091.1:p.Cys244Trp
NM_181426.2:c.732T>G MANE Select NP_852091.1:p.Cys244Trp
Search 100 bp 5'
Search 100 bp 3'