Canonical Allele Identifier: CA2716111
Gene: CCDC39 HGNC NCBI

Linked Data

dbSNP Id: rs775142858

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659529G>C , CM000665.2:g.180659529G>C GRCh38
NC_000003.11:g.180377317G>C , CM000665.1:g.180377317G>C GRCh37
NC_000003.10:g.181860011G>C NCBI36
NG_029581.1:g.24967C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.661C>G MANE Select ENSP00000417960.2:p.Gln221Glu
ENST00000650641.1:n.740C>G
ENST00000650889.1:n.833C>G
ENST00000651046.1:c.661C>G ENSP00000499175.1:p.Gln221Glu
ENST00000651818.1:n.803C>G
ENST00000652024.1:n.752C>G
ENST00000652408.1:n.798C>G
ENST00000442201.6:c.661C>G ENSP00000405708.2:p.Gln221Glu
ENST00000476379.5:c.661C>G ENSP00000417960.1:p.Gln221Glu
NM_181426.1:c.661C>G NP_852091.1:p.Gln221Glu
NM_181426.2:c.661C>G MANE Select NP_852091.1:p.Gln221Glu