Canonical Allele Identifier: CA2715640

Gene: CCDC39 TTC14

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180616537G>T , CM000665.2:g.180616537G>T	GRCh38
NC_000003.11:g.180334325G>T , CM000665.1:g.180334325G>T	GRCh37
NC_000003.10:g.181817019G>T	NCBI36
NG_029581.1:g.67959C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.2565C>A (CCDC39) MANE Select	NP_852091.1:p.Ile855=
ENST00000476379.6:c.2565C>A (CCDC39) MANE Select	ENSP00000417960.2:p.Ile855=
NM_001288582.1:c.1775-843G>T (TTC14)	NP_001275511.1:n.1775-843G>T
NM_001288582.2:c.1775-843G>T (TTC14)	NP_001275511.1:n.1775-843G>T
NM_181426.1:c.2565C>A (CCDC39)	NP_852091.1:p.Ile855=
ENST00000382584.8:c.1775-843G>T (TTC14)	ENSP00000372027.4:n.1775-843G>T
ENST00000442201.6:c.2565C>A	ENSP00000405708.2:p.Ile855=
ENST00000473854.5:c.116C>A
ENST00000476379.5:c.*389C>A	ENSP00000417960.1:n.*389C>A
ENST00000489868.5:c.81C>A	ENSP00000420025.1:p.Ile27=
ENST00000489868.6:c.81C>A (CCDC39)	ENSP00000420025.1:p.Ile27=
ENST00000651046.1:c.2373C>A (CCDC39)	ENSP00000499175.1:p.Ile791=
ENST00000651922.1:n.1890C>A (CCDC39)
ENST00000652010.1:n.2641C>A (CCDC39)