Canonical Allele Identifier: CA2624689714

Gene: TOGARAM1

Linked Data

• gnomAD v4: 14-45073749-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073749A>C , CM000676.2:g.45073749A>C	GRCh38
NC_000014.8:g.45542952A>C , CM000676.1:g.45542952A>C	GRCh37
NC_000014.7:g.44612702A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*188A>C MANE Select	ENSP00000354917.2:n.*188A>C
ENST00000361462.6:c.*188A>C	ENSP00000354917.2:n.*188A>C
ENST00000361577.7:c.*188A>C	ENSP00000355045.3:n.*188A>C
ENST00000556823.1:c.656A>C	ENSP00000450465.1:n.656A>C
ENST00000557423.5:c.*2353A>C	ENSP00000451829.1:n.*2353A>C
NM_001308120.1:c.*188A>C	NP_001295049.1:n.*188A>C
NM_015091.2:c.*188A>C	NP_055906.2:n.*188A>C
NM_015091.3:c.*188A>C	NP_055906.2:n.*188A>C
NR_131765.1:n.5573A>C
XM_011536571.1:c.*493A>C	XP_011534873.1:n.*493A>C
XM_017021098.1:c.*188A>C	XP_016876587.1:n.*188A>C
XM_017021099.1:c.*188A>C	XP_016876588.1:n.*188A>C
XR_001750194.1:n.5837A>C
XR_001750195.1:n.5480A>C
NM_001308120.2:c.*188A>C MANE Select	NP_001295049.1:n.*188A>C
NM_015091.4:c.*188A>C	NP_055906.2:n.*188A>C
NR_131765.2:n.5573A>C