Canonical Allele Identifier: CA88644763

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180648299G>A , CM000665.2:g.180648299G>A	GRCh38
NC_000003.11:g.180366087G>A , CM000665.1:g.180366087G>A	GRCh37
NC_000003.10:g.181848781G>A	NCBI36
NG_029581.1:g.36197C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.1228C>T MANE Select	NP_852091.1:p.Gln410Ter
ENST00000476379.6:c.1228C>T MANE Select	ENSP00000417960.2:p.Gln410Ter
NM_181426.1:c.1228C>T	NP_852091.1:p.Gln410Ter
ENST00000442201.6:c.1228C>T	ENSP00000405708.2:p.Gln410Ter
ENST00000476379.5:c.1228C>T	ENSP00000417960.1:p.Gln410Ter
ENST00000650641.1:n.1115C>T
ENST00000650889.1:n.1619C>T
ENST00000651046.1:c.1036C>T	ENSP00000499175.1:p.Gln346Ter
ENST00000651818.1:n.1178C>T
ENST00000651922.1:n.553C>T
ENST00000652024.1:n.1127C>T
ENST00000652408.1:n.1365C>T