Canonical Allele Identifier: CA2133565740

Gene: TOGARAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073781C= , CM000676.2:g.45073781C=	GRCh38
NC_000014.8:g.45542984C= , CM000676.1:g.45542984C=	GRCh37
NC_000014.7:g.44612734C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361462.7:c.*220C= MANE Select	ENSP00000354917.2:n.*220C=
ENST00000361462.6:c.*220C=	ENSP00000354917.2:n.*220C=
ENST00000361577.7:c.*220C=	ENSP00000355045.3:n.*220C=
ENST00000556823.1:c.688C=	ENSP00000450465.1:n.688C=
ENST00000557423.5:c.*2385C=	ENSP00000451829.1:n.*2385C=
NM_001308120.1:c.*220C=	NP_001295049.1:n.*220C=
NM_015091.2:c.*220C=	NP_055906.2:n.*220C=
NM_015091.3:c.*220C=	NP_055906.2:n.*220C=
NR_131765.1:n.5605C=
XM_011536571.1:c.*525C=	XP_011534873.1:n.*525C=
XM_017021098.1:c.*220C=	XP_016876587.1:n.*220C=
XM_017021099.1:c.*220C=	XP_016876588.1:n.*220C=
XR_001750194.1:n.5869C=
XR_001750195.1:n.5512C=
NM_001308120.2:c.*220C= MANE Select	NP_001295049.1:n.*220C=
NM_015091.4:c.*220C=	NP_055906.2:n.*220C=
NR_131765.2:n.5605C=