Canonical Allele Identifier: CA259603167

Gene: TOGARAM1

Linked Data

• dbSNP Id: rs545179783
• gnomAD v3: 14-45073774-A-G
• gnomAD v4: 14-45073774-A-G
• MyVariant Identifiers: chr14:g.45542977A>G (hg19) ; chr14:g.45073774A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073774A>G , CM000676.2:g.45073774A>G	GRCh38
NC_000014.8:g.45542977A>G , CM000676.1:g.45542977A>G	GRCh37
NC_000014.7:g.44612727A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*213A>G MANE Select	ENSP00000354917.2:n.*213A>G
ENST00000361462.6:c.*213A>G	ENSP00000354917.2:n.*213A>G
ENST00000361577.7:c.*213A>G	ENSP00000355045.3:n.*213A>G
ENST00000556823.1:c.681A>G	ENSP00000450465.1:n.681A>G
ENST00000557423.5:c.*2378A>G	ENSP00000451829.1:n.*2378A>G
NM_001308120.1:c.*213A>G	NP_001295049.1:n.*213A>G
NM_015091.2:c.*213A>G	NP_055906.2:n.*213A>G
NM_015091.3:c.*213A>G	NP_055906.2:n.*213A>G
NR_131765.1:n.5598A>G
XM_011536571.1:c.*518A>G	XP_011534873.1:n.*518A>G
XM_017021098.1:c.*213A>G	XP_016876587.1:n.*213A>G
XM_017021099.1:c.*213A>G	XP_016876588.1:n.*213A>G
XR_001750194.1:n.5862A>G
XR_001750195.1:n.5505A>G
NM_001308120.2:c.*213A>G MANE Select	NP_001295049.1:n.*213A>G
NM_015091.4:c.*213A>G	NP_055906.2:n.*213A>G
NR_131765.2:n.5598A>G