Canonical Allele Identifier: CA2531871464

Gene: TOGARAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073852A>T , CM000676.2:g.45073852A>T	GRCh38
NC_000014.8:g.45543055A>T , CM000676.1:g.45543055A>T	GRCh37
NC_000014.7:g.44612805A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*291A>T MANE Select	ENSP00000354917.2:n.*291A>T
ENST00000361462.6:c.*291A>T	ENSP00000354917.2:n.*291A>T
ENST00000361577.7:c.*291A>T	ENSP00000355045.3:n.*291A>T
ENST00000557423.5:c.*2456A>T	ENSP00000451829.1:n.*2456A>T
NM_001308120.1:c.*291A>T	NP_001295049.1:n.*291A>T
NM_015091.2:c.*291A>T	NP_055906.2:n.*291A>T
NM_015091.3:c.*291A>T	NP_055906.2:n.*291A>T
NR_131765.1:n.5676A>T
XM_011536571.1:c.*596A>T	XP_011534873.1:n.*596A>T
XM_017021098.1:c.*291A>T	XP_016876587.1:n.*291A>T
XM_017021099.1:c.*291A>T	XP_016876588.1:n.*291A>T
XR_001750194.1:n.5940A>T
XR_001750195.1:n.5583A>T
NM_001308120.2:c.*291A>T MANE Select	NP_001295049.1:n.*291A>T
NM_015091.4:c.*291A>T	NP_055906.2:n.*291A>T
NR_131765.2:n.5676A>T