Canonical Allele Identifier: CA2668664470

Gene: CCDC39

Linked Data

• gnomAD v4: 3-180659855-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659855C>A , CM000665.2:g.180659855C>A	GRCh38
NC_000003.11:g.180377643C>A , CM000665.1:g.180377643C>A	GRCh37
NC_000003.10:g.181860337C>A	NCBI36
NG_029581.1:g.24641G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-86G>T MANE Select	ENSP00000417960.2:n.517-86G>T
ENST00000650641.1:n.596-86G>T
ENST00000650889.1:n.689-86G>T
ENST00000651046.1:c.517-86G>T	ENSP00000499175.1:n.517-86G>T
ENST00000651818.1:n.659-86G>T
ENST00000652024.1:n.608-86G>T
ENST00000652408.1:n.654-86G>T
ENST00000442201.6:c.517-86G>T	ENSP00000405708.2:n.517-86G>T
ENST00000476379.5:c.517-86G>T	ENSP00000417960.1:n.517-86G>T
NM_181426.1:c.517-86G>T	NP_852091.1:n.517-86G>T
NM_181426.2:c.517-86G>T MANE Select	NP_852091.1:n.517-86G>T