Canonical Allele Identifier: CA355304543
Community Standard Title: NM_181426.2(CCDC39):c.95C>G (p.Ser32Ter)
Gene: CCDC39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180663982G>C , CM000665.2:g.180663982G>C GRCh38
NC_000003.11:g.180381770G>C , CM000665.1:g.180381770G>C GRCh37
NC_000003.10:g.181864464G>C NCBI36
NG_029581.1:g.20514C>G

Transcript Alleles

HGVS Amino-acid Change
NM_181426.2:c.95C>G MANE Select NP_852091.1:p.Ser32Ter
ENST00000476379.6:c.95C>G MANE Select ENSP00000417960.2:p.Ser32Ter
NM_181426.1:c.95C>G NP_852091.1:p.Ser32Ter
ENST00000442201.6:c.95C>G ENSP00000405708.2:p.Ser32Ter
ENST00000471307.6:c.41C>G ENSP00000418702.2:p.Ser14Ter
ENST00000476379.5:c.95C>G ENSP00000417960.1:p.Ser32Ter
ENST00000650641.1:n.174C>G
ENST00000650889.1:n.267C>G
ENST00000651046.1:c.95C>G ENSP00000499175.1:p.Ser32Ter
ENST00000651818.1:n.237C>G
ENST00000652024.1:n.186C>G
ENST00000652408.1:n.232C>G