Canonical Allele Identifier: CA355305622

Gene: CCDC39 TTC14

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180616882G>A , CM000665.2:g.180616882G>A	GRCh38
NC_000003.11:g.180334670G>A , CM000665.1:g.180334670G>A	GRCh37
NC_000003.10:g.181817364G>A	NCBI36
NG_029581.1:g.67614C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.2350C>T (CCDC39) MANE Select	NP_852091.1:p.Gln784Ter
ENST00000476379.6:c.2350C>T (CCDC39) MANE Select	ENSP00000417960.2:p.Gln784Ter
NM_001288582.1:c.1775-498G>A (TTC14)	NP_001275511.1:n.1775-498G>A
NM_001288582.2:c.1775-498G>A (TTC14)	NP_001275511.1:n.1775-498G>A
NM_181426.1:c.2350C>T (CCDC39)	NP_852091.1:p.Gln784Ter
ENST00000382584.8:c.1775-498G>A (TTC14)	ENSP00000372027.4:n.1775-498G>A
ENST00000442201.6:c.2350C>T	ENSP00000405708.2:p.Gln784Ter
ENST00000476379.5:c.*174C>T	ENSP00000417960.1:n.*174C>T
ENST00000651046.1:c.2158C>T (CCDC39)	ENSP00000499175.1:p.Gln720Ter
ENST00000651922.1:n.1675C>T (CCDC39)
ENST00000652010.1:n.2426C>T (CCDC39)