Canonical Allele Identifier: CA1424310396

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659555_180659556delinsTC , CM000665.2:g.180659555_180659556delinsTC	GRCh38
NC_000003.11:g.180377343_180377344delinsTC , CM000665.1:g.180377343_180377344delinsTC	GRCh37
NC_000003.10:g.181860037_181860038delinsTC	NCBI36
NG_029581.1:g.24940_24941delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.634_635delinsGA MANE Select	ENSP00000417960.2:p.Asp212=
ENST00000650641.1:n.713_714delinsGA
ENST00000650889.1:n.806_807delinsGA
ENST00000651046.1:c.634_635delinsGA	ENSP00000499175.1:p.Asp212=
ENST00000651818.1:n.776_777delinsGA
ENST00000652024.1:n.725_726delinsGA
ENST00000652408.1:n.771_772delinsGA
ENST00000442201.6:c.634_635delinsGA	ENSP00000405708.2:p.Asp212=
ENST00000476379.5:c.634_635delinsGA	ENSP00000417960.1:p.Asp212=
NM_181426.1:c.634_635delinsGA	NP_852091.1:p.Asp212=
NM_181426.2:c.634_635delinsGA MANE Select	NP_852091.1:p.Asp212=