Canonical Allele Identifier: CA2133565738

Gene: TOGARAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073776_45073777delinsGA , CM000676.2:g.45073776_45073777delinsGA	GRCh38
NC_000014.8:g.45542979_45542980delinsGA , CM000676.1:g.45542979_45542980delinsGA	GRCh37
NC_000014.7:g.44612729_44612730delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*215_*216delinsGA MANE Select	ENSP00000354917.2:n.*215_*216delinsGA
ENST00000361462.6:c.*215_*216delinsGA	ENSP00000354917.2:n.*215_*216delinsGA
ENST00000361577.7:c.*215_*216delinsGA	ENSP00000355045.3:n.*215_*216delinsGA
ENST00000556823.1:c.683_684delinsGA	ENSP00000450465.1:n.683_684delinsGA
ENST00000557423.5:c.*2380_*2381delinsGA	ENSP00000451829.1:n.*2380_*2381delinsGA
NM_001308120.1:c.*215_*216delinsGA	NP_001295049.1:n.*215_*216delinsGA
NM_015091.2:c.*215_*216delinsGA	NP_055906.2:n.*215_*216delinsGA
NM_015091.3:c.*215_*216delinsGA	NP_055906.2:n.*215_*216delinsGA
NR_131765.1:n.5600_5601delinsGA
XM_011536571.1:c.*520_*521delinsGA	XP_011534873.1:n.*520_*521delinsGA
XM_017021098.1:c.*215_*216delinsGA	XP_016876587.1:n.*215_*216delinsGA
XM_017021099.1:c.*215_*216delinsGA	XP_016876588.1:n.*215_*216delinsGA
XR_001750194.1:n.5864_5865delinsGA
XR_001750195.1:n.5507_5508delinsGA
NM_001308120.2:c.*215_*216delinsGA MANE Select	NP_001295049.1:n.*215_*216delinsGA
NM_015091.4:c.*215_*216delinsGA	NP_055906.2:n.*215_*216delinsGA
NR_131765.2:n.5600_5601delinsGA