Canonical Allele Identifier: CA1424310571

Gene: CCDC39

Linked Data

• dbSNP Id: rs1711700835
• gnomAD v4: 3-180659896-TAATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659901_180659904del , CM000665.2:g.180659901_180659904del	GRCh38
NC_000003.11:g.180377689_180377692del , CM000665.1:g.180377689_180377692del	GRCh37
NC_000003.10:g.181860383_181860386del	NCBI36
NG_029581.1:g.24596_24599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-131_517-128del MANE Select	ENSP00000417960.2:n.517-131_517-128del
ENST00000650641.1:n.596-131_596-128del
ENST00000650889.1:n.689-131_689-128del
ENST00000651046.1:c.517-131_517-128del	ENSP00000499175.1:n.517-131_517-128del
ENST00000651818.1:n.659-131_659-128del
ENST00000652024.1:n.608-131_608-128del
ENST00000652408.1:n.654-131_654-128del
ENST00000442201.6:c.517-131_517-128del	ENSP00000405708.2:n.517-131_517-128del
ENST00000476379.5:c.517-131_517-128del	ENSP00000417960.1:n.517-131_517-128del
NM_181426.1:c.517-131_517-128del	NP_852091.1:n.517-131_517-128del
NM_181426.2:c.517-131_517-128del MANE Select	NP_852091.1:n.517-131_517-128del