Canonical Allele Identifier: CA706123768

Gene: TOGARAM1

Linked Data

• dbSNP Id: rs1453952526
• MyVariant Identifiers: chr14:g.45543093G>A (hg19) ; chr14:g.45073890G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073890G>A , CM000676.2:g.45073890G>A	GRCh38
NC_000014.8:g.45543093G>A , CM000676.1:g.45543093G>A	GRCh37
NC_000014.7:g.44612843G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*329G>A MANE Select	ENSP00000354917.2:n.*329G>A
ENST00000361462.6:c.*329G>A	ENSP00000354917.2:n.*329G>A
ENST00000361577.7:c.*329G>A	ENSP00000355045.3:n.*329G>A
ENST00000557423.5:c.*2494G>A	ENSP00000451829.1:n.*2494G>A
NM_001308120.1:c.*329G>A	NP_001295049.1:n.*329G>A
NM_015091.2:c.*329G>A	NP_055906.2:n.*329G>A
NM_015091.3:c.*329G>A	NP_055906.2:n.*329G>A
NR_131765.1:n.5714G>A
XM_011536571.1:c.*634G>A	XP_011534873.1:n.*634G>A
XM_017021098.1:c.*329G>A	XP_016876587.1:n.*329G>A
XM_017021099.1:c.*329G>A	XP_016876588.1:n.*329G>A
XR_001750194.1:n.5978G>A
XR_001750195.1:n.5621G>A
NM_001308120.2:c.*329G>A MANE Select	NP_001295049.1:n.*329G>A
NM_015091.4:c.*329G>A	NP_055906.2:n.*329G>A
NR_131765.2:n.5714G>A