Canonical Allele Identifier: CA1424310576

Gene: CCDC39

Linked Data

• dbSNP Id: rs1711701148
• gnomAD v4: 3-180659907-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659910_180659912del , CM000665.2:g.180659910_180659912del	GRCh38
NC_000003.11:g.180377698_180377700del , CM000665.1:g.180377698_180377700del	GRCh37
NC_000003.10:g.181860392_181860394del	NCBI36
NG_029581.1:g.24586_24588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-141_517-139del MANE Select	ENSP00000417960.2:n.517-141_517-139del
ENST00000650641.1:n.596-141_596-139del
ENST00000650889.1:n.689-141_689-139del
ENST00000651046.1:c.517-141_517-139del	ENSP00000499175.1:n.517-141_517-139del
ENST00000651818.1:n.659-141_659-139del
ENST00000652024.1:n.608-141_608-139del
ENST00000652408.1:n.654-141_654-139del
ENST00000442201.6:c.517-141_517-139del	ENSP00000405708.2:n.517-141_517-139del
ENST00000476379.5:c.517-141_517-139del	ENSP00000417960.1:n.517-141_517-139del
NM_181426.1:c.517-141_517-139del	NP_852091.1:n.517-141_517-139del
NM_181426.2:c.517-141_517-139del MANE Select	NP_852091.1:n.517-141_517-139del