Canonical Allele Identifier: CA2508349731

Gene: TOGARAM1

Linked Data

• dbSNP Id: rs2139016962

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073879A>C , CM000676.2:g.45073879A>C	GRCh38
NC_000014.8:g.45543082A>C , CM000676.1:g.45543082A>C	GRCh37
NC_000014.7:g.44612832A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361462.7:c.*318A>C MANE Select	ENSP00000354917.2:n.*318A>C
ENST00000361462.6:c.*318A>C	ENSP00000354917.2:n.*318A>C
ENST00000361577.7:c.*318A>C	ENSP00000355045.3:n.*318A>C
ENST00000557423.5:c.*2483A>C	ENSP00000451829.1:n.*2483A>C
NM_001308120.1:c.*318A>C	NP_001295049.1:n.*318A>C
NM_015091.2:c.*318A>C	NP_055906.2:n.*318A>C
NM_015091.3:c.*318A>C	NP_055906.2:n.*318A>C
NR_131765.1:n.5703A>C
XM_011536571.1:c.*623A>C	XP_011534873.1:n.*623A>C
XM_017021098.1:c.*318A>C	XP_016876587.1:n.*318A>C
XM_017021099.1:c.*318A>C	XP_016876588.1:n.*318A>C
XR_001750194.1:n.5967A>C
XR_001750195.1:n.5610A>C
NM_001308120.2:c.*318A>C MANE Select	NP_001295049.1:n.*318A>C
NM_015091.4:c.*318A>C	NP_055906.2:n.*318A>C
NR_131765.2:n.5703A>C