Canonical Allele Identifier: CA2133565717

Gene: TOGARAM1

Linked Data

• dbSNP Id: rs1883486847
• gnomAD v4: 14-45073741-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073741C>T , CM000676.2:g.45073741C>T	GRCh38
NC_000014.8:g.45542944C>T , CM000676.1:g.45542944C>T	GRCh37
NC_000014.7:g.44612694C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*180C>T MANE Select	ENSP00000354917.2:n.*180C>T
ENST00000361462.6:c.*180C>T	ENSP00000354917.2:n.*180C>T
ENST00000361577.7:c.*180C>T	ENSP00000355045.3:n.*180C>T
ENST00000556823.1:c.648C>T	ENSP00000450465.1:n.648C>T
ENST00000557423.5:c.*2345C>T	ENSP00000451829.1:n.*2345C>T
NM_001308120.1:c.*180C>T	NP_001295049.1:n.*180C>T
NM_015091.2:c.*180C>T	NP_055906.2:n.*180C>T
NM_015091.3:c.*180C>T	NP_055906.2:n.*180C>T
NR_131765.1:n.5565C>T
XM_011536571.1:c.*485C>T	XP_011534873.1:n.*485C>T
XM_017021098.1:c.*180C>T	XP_016876587.1:n.*180C>T
XM_017021099.1:c.*180C>T	XP_016876588.1:n.*180C>T
XR_001750194.1:n.5829C>T
XR_001750195.1:n.5472C>T
NM_001308120.2:c.*180C>T MANE Select	NP_001295049.1:n.*180C>T
NM_015091.4:c.*180C>T	NP_055906.2:n.*180C>T
NR_131765.2:n.5565C>T