Canonical Allele Identifier: CA2838536814

Gene: TEX29

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.111321004_111321005insGAGCGGGGGGGGGGGGG , CM000675.2:g.111321004_111321005insGAGCGGGGGGGGGGGGG	GRCh38
NC_000013.10:g.111973351_111973352insGAGCGGGGGGGGGGGGG , CM000675.1:g.111973351_111973352insGAGCGGGGGGGGGGGGG	GRCh37
NC_000013.9:g.110771352_110771353insGAGCGGGGGGGGGGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283547.2:c.58+56_58+57insGAGCGGGGGGGGGGGGG MANE Select	ENSP00000283547.1:n.58+56_58+57insGAGCGGGGGGGGGGGGG
ENST00000283547.1:c.58+56_58+57insGAGCGGGGGGGGGGGGG	ENSP00000283547.1:n.58+56_58+57insGAGCGGGGGGGGGGGGG
ENST00000497241.5:c.139+56_139+57insGAGCGGGGGGGGGGGGG	ENSP00000431661.1:n.139+56_139+57insGAGCGGGGGGGGGGGGG
NM_001303133.1:c.-19+56_-19+57insGAGCGGGGGGGGGGGGG	NP_001290062.1:n.-19+56_-19+57insGAGCGGGGGGGGGGGGG
NM_152324.2:c.58+56_58+57insGAGCGGGGGGGGGGGGG	NP_689537.1:n.58+56_58+57insGAGCGGGGGGGGGGGGG
XM_017020387.1:c.298+56_298+57insGAGCGGGGGGGGGGGGG	XP_016875876.1:n.298+56_298+57insGAGCGGGGGGGGGGGGG
XM_017020388.1:c.139+56_139+57insGAGCGGGGGGGGGGGGG	XP_016875877.1:n.139+56_139+57insGAGCGGGGGGGGGGGGG
XR_001749478.1:n.1525+56_1525+57insGAGCGGGGGGGGGGGGG
NM_152324.3:c.58+56_58+57insGAGCGGGGGGGGGGGGG MANE Select	NP_689537.1:n.58+56_58+57insGAGCGGGGGGGGGGGGG