Canonical Allele Identifier: CA2668664436

Gene: CCDC39

Linked Data

• gnomAD v4: 3-180659786-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659788_180659789del , CM000665.2:g.180659788_180659789del	GRCh38
NC_000003.11:g.180377576_180377577del , CM000665.1:g.180377576_180377577del	GRCh37
NC_000003.10:g.181860270_181860271del	NCBI36
NG_029581.1:g.24708_24709del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-19_517-18del MANE Select	ENSP00000417960.2:n.517-19_517-18del
ENST00000650641.1:n.596-19_596-18del
ENST00000650889.1:n.689-19_689-18del
ENST00000651046.1:c.517-19_517-18del	ENSP00000499175.1:n.517-19_517-18del
ENST00000651818.1:n.659-19_659-18del
ENST00000652024.1:n.608-19_608-18del
ENST00000652408.1:n.654-19_654-18del
ENST00000442201.6:c.517-19_517-18del	ENSP00000405708.2:n.517-19_517-18del
ENST00000476379.5:c.517-19_517-18del	ENSP00000417960.1:n.517-19_517-18del
NM_181426.1:c.517-19_517-18del	NP_852091.1:n.517-19_517-18del
NM_181426.2:c.517-19_517-18del MANE Select	NP_852091.1:n.517-19_517-18del