Canonical Allele Identifier: CA2516377103

Gene: TOGARAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073863dup , CM000676.2:g.45073863dup	GRCh38
NC_000014.8:g.45543066dup , CM000676.1:g.45543066dup	GRCh37
NC_000014.7:g.44612816dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*302dup MANE Select	ENSP00000354917.2:n.*302dup
ENST00000361462.6:c.*302dup	ENSP00000354917.2:n.*302dup
ENST00000361577.7:c.*302dup	ENSP00000355045.3:n.*302dup
ENST00000557423.5:c.*2467dup	ENSP00000451829.1:n.*2467dup
NM_001308120.1:c.*302dup	NP_001295049.1:n.*302dup
NM_015091.2:c.*302dup	NP_055906.2:n.*302dup
NM_015091.3:c.*302dup	NP_055906.2:n.*302dup
NR_131765.1:n.5687dup
XM_011536571.1:c.*607dup	XP_011534873.1:n.*607dup
XM_017021098.1:c.*302dup	XP_016876587.1:n.*302dup
XM_017021099.1:c.*302dup	XP_016876588.1:n.*302dup
XR_001750194.1:n.5951dup
XR_001750195.1:n.5594dup
NM_001308120.2:c.*302dup MANE Select	NP_001295049.1:n.*302dup
NM_015091.4:c.*302dup	NP_055906.2:n.*302dup
NR_131765.2:n.5687dup