Canonical Allele Identifier: CA2801407709

Gene: TOGARAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073750dup , CM000676.2:g.45073750dup	GRCh38
NC_000014.8:g.45542953dup , CM000676.1:g.45542953dup	GRCh37
NC_000014.7:g.44612703dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*189dup MANE Select	ENSP00000354917.2:n.*189dup
ENST00000361462.6:c.*189dup	ENSP00000354917.2:n.*189dup
ENST00000361577.7:c.*189dup	ENSP00000355045.3:n.*189dup
ENST00000556823.1:c.657dup	ENSP00000450465.1:n.657dup
ENST00000557423.5:c.*2354dup	ENSP00000451829.1:n.*2354dup
NM_001308120.1:c.*189dup	NP_001295049.1:n.*189dup
NM_015091.2:c.*189dup	NP_055906.2:n.*189dup
NM_015091.3:c.*189dup	NP_055906.2:n.*189dup
NR_131765.1:n.5574dup
XM_011536571.1:c.*494dup	XP_011534873.1:n.*494dup
XM_017021098.1:c.*189dup	XP_016876587.1:n.*189dup
XM_017021099.1:c.*189dup	XP_016876588.1:n.*189dup
XR_001750194.1:n.5838dup
XR_001750195.1:n.5481dup
NM_001308120.2:c.*189dup MANE Select	NP_001295049.1:n.*189dup
NM_015091.4:c.*189dup	NP_055906.2:n.*189dup
NR_131765.2:n.5574dup