Canonical Allele Identifier: CA1424310548

Gene: CCDC39

Linked Data

• dbSNP Id: rs1711699550
• gnomAD v4: 3-180659862-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659862C>T , CM000665.2:g.180659862C>T	GRCh38
NC_000003.11:g.180377650C>T , CM000665.1:g.180377650C>T	GRCh37
NC_000003.10:g.181860344C>T	NCBI36
NG_029581.1:g.24634G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-93G>A MANE Select	ENSP00000417960.2:n.517-93G>A
ENST00000650641.1:n.596-93G>A
ENST00000650889.1:n.689-93G>A
ENST00000651046.1:c.517-93G>A	ENSP00000499175.1:n.517-93G>A
ENST00000651818.1:n.659-93G>A
ENST00000652024.1:n.608-93G>A
ENST00000652408.1:n.654-93G>A
ENST00000442201.6:c.517-93G>A	ENSP00000405708.2:n.517-93G>A
ENST00000476379.5:c.517-93G>A	ENSP00000417960.1:n.517-93G>A
NM_181426.1:c.517-93G>A	NP_852091.1:n.517-93G>A
NM_181426.2:c.517-93G>A MANE Select	NP_852091.1:n.517-93G>A