Canonical Allele Identifier: CA2624689791

Gene: TOGARAM1

Linked Data

• gnomAD v4: 14-45073895-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073895T>A , CM000676.2:g.45073895T>A	GRCh38
NC_000014.8:g.45543098T>A , CM000676.1:g.45543098T>A	GRCh37
NC_000014.7:g.44612848T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361462.7:c.*334T>A MANE Select	ENSP00000354917.2:n.*334T>A
ENST00000361462.6:c.*334T>A	ENSP00000354917.2:n.*334T>A
ENST00000361577.7:c.*334T>A	ENSP00000355045.3:n.*334T>A
ENST00000557423.5:c.*2499T>A	ENSP00000451829.1:n.*2499T>A
NM_001308120.1:c.*334T>A	NP_001295049.1:n.*334T>A
NM_015091.2:c.*334T>A	NP_055906.2:n.*334T>A
NM_015091.3:c.*334T>A	NP_055906.2:n.*334T>A
NR_131765.1:n.5719T>A
XM_011536571.1:c.*639T>A	XP_011534873.1:n.*639T>A
XM_017021098.1:c.*334T>A	XP_016876587.1:n.*334T>A
XM_017021099.1:c.*334T>A	XP_016876588.1:n.*334T>A
XR_001750194.1:n.5983T>A
XR_001750195.1:n.5626T>A
NM_001308120.2:c.*334T>A MANE Select	NP_001295049.1:n.*334T>A
NM_015091.4:c.*334T>A	NP_055906.2:n.*334T>A
NR_131765.2:n.5719T>A