Canonical Allele Identifier: CA2624689730

Gene: TOGARAM1

Linked Data

• gnomAD v4: 14-45073770-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073772del , CM000676.2:g.45073772del	GRCh38
NC_000014.8:g.45542975del , CM000676.1:g.45542975del	GRCh37
NC_000014.7:g.44612725del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*211del MANE Select	ENSP00000354917.2:n.*211del
ENST00000361462.6:c.*211del	ENSP00000354917.2:n.*211del
ENST00000361577.7:c.*211del	ENSP00000355045.3:n.*211del
ENST00000556823.1:c.679del	ENSP00000450465.1:n.679del
ENST00000557423.5:c.*2376del	ENSP00000451829.1:n.*2376del
NM_001308120.1:c.*211del	NP_001295049.1:n.*211del
NM_015091.2:c.*211del	NP_055906.2:n.*211del
NM_015091.3:c.*211del	NP_055906.2:n.*211del
NR_131765.1:n.5596del
XM_011536571.1:c.*516del	XP_011534873.1:n.*516del
XM_017021098.1:c.*211del	XP_016876587.1:n.*211del
XM_017021099.1:c.*211del	XP_016876588.1:n.*211del
XR_001750194.1:n.5860del
XR_001750195.1:n.5503del
NM_001308120.2:c.*211del MANE Select	NP_001295049.1:n.*211del
NM_015091.4:c.*211del	NP_055906.2:n.*211del
NR_131765.2:n.5596del