Canonical Allele Identifier: CA88644682

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180648171G>T , CM000665.2:g.180648171G>T	GRCh38
NC_000003.11:g.180365959G>T , CM000665.1:g.180365959G>T	GRCh37
NC_000003.10:g.181848653G>T	NCBI36
NG_029581.1:g.36325C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.1356C>A MANE Select	NP_852091.1:p.Tyr452Ter
ENST00000476379.6:c.1356C>A MANE Select	ENSP00000417960.2:p.Tyr452Ter
NM_181426.1:c.1356C>A	NP_852091.1:p.Tyr452Ter
ENST00000442201.6:c.1356C>A	ENSP00000405708.2:p.Tyr452Ter
ENST00000476379.5:c.1356C>A	ENSP00000417960.1:p.Tyr452Ter
ENST00000650641.1:n.1243C>A
ENST00000650889.1:n.1747C>A
ENST00000651046.1:c.1164C>A	ENSP00000499175.1:p.Tyr388Ter
ENST00000651818.1:n.1306C>A
ENST00000651922.1:n.681C>A
ENST00000652024.1:n.1255C>A
ENST00000652408.1:n.1493C>A