Canonical Allele Identifier: CA2133565792

Gene: TOGARAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073860A= , CM000676.2:g.45073860A=	GRCh38
NC_000014.8:g.45543063A= , CM000676.1:g.45543063A=	GRCh37
NC_000014.7:g.44612813A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*299A= MANE Select	ENSP00000354917.2:n.*299A=
ENST00000361462.6:c.*299A=	ENSP00000354917.2:n.*299A=
ENST00000361577.7:c.*299A=	ENSP00000355045.3:n.*299A=
ENST00000557423.5:c.*2464A=	ENSP00000451829.1:n.*2464A=
NM_001308120.1:c.*299A=	NP_001295049.1:n.*299A=
NM_015091.2:c.*299A=	NP_055906.2:n.*299A=
NM_015091.3:c.*299A=	NP_055906.2:n.*299A=
NR_131765.1:n.5684A=
XM_011536571.1:c.*604A=	XP_011534873.1:n.*604A=
XM_017021098.1:c.*299A=	XP_016876587.1:n.*299A=
XM_017021099.1:c.*299A=	XP_016876588.1:n.*299A=
XR_001750194.1:n.5948A=
XR_001750195.1:n.5591A=
NM_001308120.2:c.*299A= MANE Select	NP_001295049.1:n.*299A=
NM_015091.4:c.*299A=	NP_055906.2:n.*299A=
NR_131765.2:n.5684A=