Canonical Allele Identifier: CA903358463

Gene: CCDC39

Linked Data

• dbSNP Id: rs1298926936
• gnomAD v3: 3-180659904-ATC-A
• gnomAD v4: 3-180659904-ATC-A
• MyVariant Identifiers: chr3:g.180377693_180377694del (hg19) ; chr3:g.180659905_180659906del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659906_180659907del , CM000665.2:g.180659906_180659907del	GRCh38
NC_000003.11:g.180377694_180377695del , CM000665.1:g.180377694_180377695del	GRCh37
NC_000003.10:g.181860388_181860389del	NCBI36
NG_029581.1:g.24590_24591del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-137_517-136del MANE Select	ENSP00000417960.2:n.517-137_517-136del
ENST00000650641.1:n.596-137_596-136del
ENST00000650889.1:n.689-137_689-136del
ENST00000651046.1:c.517-137_517-136del	ENSP00000499175.1:n.517-137_517-136del
ENST00000651818.1:n.659-137_659-136del
ENST00000652024.1:n.608-137_608-136del
ENST00000652408.1:n.654-137_654-136del
ENST00000442201.6:c.517-137_517-136del	ENSP00000405708.2:n.517-137_517-136del
ENST00000476379.5:c.517-137_517-136del	ENSP00000417960.1:n.517-137_517-136del
NM_181426.1:c.517-137_517-136del	NP_852091.1:n.517-137_517-136del
NM_181426.2:c.517-137_517-136del MANE Select	NP_852091.1:n.517-137_517-136del