Canonical Allele Identifier: CA2577967087

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659624_180659630del , CM000665.2:g.180659624_180659630del	GRCh38
NC_000003.11:g.180377412_180377418del , CM000665.1:g.180377412_180377418del	GRCh37
NC_000003.10:g.181860106_181860112del	NCBI36
NG_029581.1:g.24866_24872del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.609+47_610-44del MANE Select	ENSP00000417960.2:n.609+47_610-44del
ENST00000650641.1:n.688+47_689-44del
ENST00000650889.1:n.781+47_782-44del
ENST00000651046.1:c.609+47_610-44del	ENSP00000499175.1:n.609+47_610-44del
ENST00000651818.1:n.751+47_752-44del
ENST00000652024.1:n.700+47_701-44del
ENST00000652408.1:n.746+47_747-44del
ENST00000442201.6:c.609+47_610-44del	ENSP00000405708.2:n.609+47_610-44del
ENST00000476379.5:c.609+47_610-44del	ENSP00000417960.1:n.609+47_610-44del
NM_181426.1:c.609+47_610-44del	NP_852091.1:n.609+47_610-44del
NM_181426.2:c.609+47_610-44del MANE Select	NP_852091.1:n.609+47_610-44del