Canonical Allele Identifier: CA2133565734

Gene: TOGARAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073774A= , CM000676.2:g.45073774A=	GRCh38
NC_000014.8:g.45542977A= , CM000676.1:g.45542977A=	GRCh37
NC_000014.7:g.44612727A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361462.7:c.*213A= MANE Select	ENSP00000354917.2:n.*213A=
ENST00000361462.6:c.*213A=	ENSP00000354917.2:n.*213A=
ENST00000361577.7:c.*213A=	ENSP00000355045.3:n.*213A=
ENST00000556823.1:c.681A=	ENSP00000450465.1:n.681A=
ENST00000557423.5:c.*2378A=	ENSP00000451829.1:n.*2378A=
NM_001308120.1:c.*213A=	NP_001295049.1:n.*213A=
NM_015091.2:c.*213A=	NP_055906.2:n.*213A=
NM_015091.3:c.*213A=	NP_055906.2:n.*213A=
NR_131765.1:n.5598A=
XM_011536571.1:c.*518A=	XP_011534873.1:n.*518A=
XM_017021098.1:c.*213A=	XP_016876587.1:n.*213A=
XM_017021099.1:c.*213A=	XP_016876588.1:n.*213A=
XR_001750194.1:n.5862A=
XR_001750195.1:n.5505A=
NM_001308120.2:c.*213A= MANE Select	NP_001295049.1:n.*213A=
NM_015091.4:c.*213A=	NP_055906.2:n.*213A=
NR_131765.2:n.5598A=