Canonical Allele Identifier: CA355302082
Gene: CCDC39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.180377293T>C (hg19) chr3:g.180659505T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.685A>G MANE Select ENSP00000417960.2:p.Asn229Asp
ENST00000650641.1:n.764A>G
ENST00000650889.1:n.857A>G
ENST00000651046.1:c.685A>G ENSP00000499175.1:p.Asn229Asp
ENST00000651818.1:n.827A>G
ENST00000652024.1:n.776A>G
ENST00000652408.1:n.822A>G
ENST00000442201.6:c.685A>G ENSP00000405708.2:p.Asn229Asp
ENST00000476379.5:c.685A>G ENSP00000417960.1:p.Asn229Asp
NM_181426.1:c.685A>G NP_852091.1:p.Asn229Asp
NM_181426.2:c.685A>G MANE Select NP_852091.1:p.Asn229Asp
Search 100 bp 5'
Search 100 bp 3'