Canonical Allele Identifier: CA2715636

Gene: CCDC39 TTC14

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180616515C>T , CM000665.2:g.180616515C>T	GRCh38
NC_000003.11:g.180334303C>T , CM000665.1:g.180334303C>T	GRCh37
NC_000003.10:g.181816997C>T	NCBI36
NG_029581.1:g.67981G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.2586+1G>A (CCDC39) MANE Select	NP_852091.1:n.2586+1G>A
ENST00000476379.6:c.2586+1G>A (CCDC39) MANE Select	ENSP00000417960.2:n.2586+1G>A
NM_001288582.1:c.1775-865C>T (TTC14)	NP_001275511.1:n.1775-865C>T
NM_001288582.2:c.1775-865C>T (TTC14)	NP_001275511.1:n.1775-865C>T
NM_181426.1:c.2586+1G>A (CCDC39)	NP_852091.1:n.2586+1G>A
ENST00000382584.8:c.1775-865C>T (TTC14)	ENSP00000372027.4:n.1775-865C>T
ENST00000442201.6:c.2586+1G>A	ENSP00000405708.2:n.2586+1G>A
ENST00000473854.5:c.137+1G>A
ENST00000476379.5:c.*410+1G>A	ENSP00000417960.1:n.*410+1G>A
ENST00000489868.5:c.102+1G>A	ENSP00000420025.1:n.102+1G>A
ENST00000489868.6:c.102+1G>A (CCDC39)	ENSP00000420025.1:n.102+1G>A
ENST00000651046.1:c.2394+1G>A (CCDC39)	ENSP00000499175.1:n.2394+1G>A
ENST00000651922.1:n.1911+1G>A (CCDC39)
ENST00000652010.1:n.2662+1G>A (CCDC39)