Canonical Allele Identifier: CA1424310501
Gene: CCDC39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659789_180659796delinsAGATACTT , CM000665.2:g.180659789_180659796delinsAGATACTT GRCh38
NC_000003.11:g.180377577_180377584delinsAGATACTT , CM000665.1:g.180377577_180377584delinsAGATACTT GRCh37
NC_000003.10:g.181860271_181860278delinsAGATACTT NCBI36
NG_029581.1:g.24700_24707delinsAAGTATCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.517-27_517-20delinsAAGTATCT MANE Select ENSP00000417960.2:n.517-27_517-20delinsAAGTATCT
ENST00000650641.1:n.596-27_596-20delinsAAGTATCT
ENST00000650889.1:n.689-27_689-20delinsAAGTATCT
ENST00000651046.1:c.517-27_517-20delinsAAGTATCT ENSP00000499175.1:n.517-27_517-20delinsAAGTATCT
ENST00000651818.1:n.659-27_659-20delinsAAGTATCT
ENST00000652024.1:n.608-27_608-20delinsAAGTATCT
ENST00000652408.1:n.654-27_654-20delinsAAGTATCT
ENST00000442201.6:c.517-27_517-20delinsAAGTATCT ENSP00000405708.2:n.517-27_517-20delinsAAGTATCT
ENST00000476379.5:c.517-27_517-20delinsAAGTATCT ENSP00000417960.1:n.517-27_517-20delinsAAGTATCT
NM_181426.1:c.517-27_517-20delinsAAGTATCT NP_852091.1:n.517-27_517-20delinsAAGTATCT
NM_181426.2:c.517-27_517-20delinsAAGTATCT MANE Select NP_852091.1:n.517-27_517-20delinsAAGTATCT