Canonical Allele Identifier: CA2668664489

Gene: CCDC39

Linked Data

• gnomAD v4: 3-180659903-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659903T>G , CM000665.2:g.180659903T>G	GRCh38
NC_000003.11:g.180377691T>G , CM000665.1:g.180377691T>G	GRCh37
NC_000003.10:g.181860385T>G	NCBI36
NG_029581.1:g.24593A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-134A>C MANE Select	ENSP00000417960.2:n.517-134A>C
ENST00000650641.1:n.596-134A>C
ENST00000650889.1:n.689-134A>C
ENST00000651046.1:c.517-134A>C	ENSP00000499175.1:n.517-134A>C
ENST00000651818.1:n.659-134A>C
ENST00000652024.1:n.608-134A>C
ENST00000652408.1:n.654-134A>C
ENST00000442201.6:c.517-134A>C	ENSP00000405708.2:n.517-134A>C
ENST00000476379.5:c.517-134A>C	ENSP00000417960.1:n.517-134A>C
NM_181426.1:c.517-134A>C	NP_852091.1:n.517-134A>C
NM_181426.2:c.517-134A>C MANE Select	NP_852091.1:n.517-134A>C