Canonical Allele Identifier: CA355301884
Gene: CCDC39 HGNC NCBI

Linked Data

gnomAD v4: 3-180659463-T-C
MyVariant Identifiers: chr3:g.180377251T>C (hg19) chr3:g.180659463T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659463T>C , CM000665.2:g.180659463T>C GRCh38
NC_000003.11:g.180377251T>C , CM000665.1:g.180377251T>C GRCh37
NC_000003.10:g.181859945T>C NCBI36
NG_029581.1:g.25033A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.727A>G MANE Select ENSP00000417960.2:p.Asn243Asp
ENST00000650641.1:n.806A>G
ENST00000650889.1:n.899A>G
ENST00000651046.1:c.727A>G ENSP00000499175.1:p.Asn243Asp
ENST00000651818.1:n.869A>G
ENST00000652024.1:n.818A>G
ENST00000652408.1:n.864A>G
ENST00000442201.6:c.727A>G ENSP00000405708.2:p.Asn243Asp
ENST00000476379.5:c.727A>G ENSP00000417960.1:p.Asn243Asp
NM_181426.1:c.727A>G NP_852091.1:p.Asn243Asp
NM_181426.2:c.727A>G MANE Select NP_852091.1:p.Asn243Asp
Search 100 bp 5'
Search 100 bp 3'