Canonical Allele Identifier: CA2133565803

Gene: TOGARAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073875T= , CM000676.2:g.45073875T=	GRCh38
NC_000014.8:g.45543078T= , CM000676.1:g.45543078T=	GRCh37
NC_000014.7:g.44612828T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*314T= MANE Select	ENSP00000354917.2:n.*314T=
ENST00000361462.6:c.*314T=	ENSP00000354917.2:n.*314T=
ENST00000361577.7:c.*314T=	ENSP00000355045.3:n.*314T=
ENST00000557423.5:c.*2479T=	ENSP00000451829.1:n.*2479T=
NM_001308120.1:c.*314T=	NP_001295049.1:n.*314T=
NM_015091.2:c.*314T=	NP_055906.2:n.*314T=
NM_015091.3:c.*314T=	NP_055906.2:n.*314T=
NR_131765.1:n.5699T=
XM_011536571.1:c.*619T=	XP_011534873.1:n.*619T=
XM_017021098.1:c.*314T=	XP_016876587.1:n.*314T=
XM_017021099.1:c.*314T=	XP_016876588.1:n.*314T=
XR_001750194.1:n.5963T=
XR_001750195.1:n.5606T=
NM_001308120.2:c.*314T= MANE Select	NP_001295049.1:n.*314T=
NM_015091.4:c.*314T=	NP_055906.2:n.*314T=
NR_131765.2:n.5699T=