Canonical Allele Identifier: CA2624689760

Gene: TOGARAM1

Linked Data

• gnomAD v4: 14-45073839-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073839C>A , CM000676.2:g.45073839C>A	GRCh38
NC_000014.8:g.45543042C>A , CM000676.1:g.45543042C>A	GRCh37
NC_000014.7:g.44612792C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*278C>A MANE Select	ENSP00000354917.2:n.*278C>A
ENST00000361462.6:c.*278C>A	ENSP00000354917.2:n.*278C>A
ENST00000361577.7:c.*278C>A	ENSP00000355045.3:n.*278C>A
ENST00000557423.5:c.*2443C>A	ENSP00000451829.1:n.*2443C>A
NM_001308120.1:c.*278C>A	NP_001295049.1:n.*278C>A
NM_015091.2:c.*278C>A	NP_055906.2:n.*278C>A
NM_015091.3:c.*278C>A	NP_055906.2:n.*278C>A
NR_131765.1:n.5663C>A
XM_011536571.1:c.*583C>A	XP_011534873.1:n.*583C>A
XM_017021098.1:c.*278C>A	XP_016876587.1:n.*278C>A
XM_017021099.1:c.*278C>A	XP_016876588.1:n.*278C>A
XR_001750194.1:n.5927C>A
XR_001750195.1:n.5570C>A
NM_001308120.2:c.*278C>A MANE Select	NP_001295049.1:n.*278C>A
NM_015091.4:c.*278C>A	NP_055906.2:n.*278C>A
NR_131765.2:n.5663C>A