Canonical Allele Identifier: CA259603178

Gene: TOGARAM1

Linked Data

• dbSNP Id: rs764387812
• MyVariant Identifiers: chr14:g.45543077A>T (hg19) ; chr14:g.45073874A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073874A>T , CM000676.2:g.45073874A>T	GRCh38
NC_000014.8:g.45543077A>T , CM000676.1:g.45543077A>T	GRCh37
NC_000014.7:g.44612827A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*313A>T MANE Select	ENSP00000354917.2:n.*313A>T
ENST00000361462.6:c.*313A>T	ENSP00000354917.2:n.*313A>T
ENST00000361577.7:c.*313A>T	ENSP00000355045.3:n.*313A>T
ENST00000557423.5:c.*2478A>T	ENSP00000451829.1:n.*2478A>T
NM_001308120.1:c.*313A>T	NP_001295049.1:n.*313A>T
NM_015091.2:c.*313A>T	NP_055906.2:n.*313A>T
NM_015091.3:c.*313A>T	NP_055906.2:n.*313A>T
NR_131765.1:n.5698A>T
XM_011536571.1:c.*618A>T	XP_011534873.1:n.*618A>T
XM_017021098.1:c.*313A>T	XP_016876587.1:n.*313A>T
XM_017021099.1:c.*313A>T	XP_016876588.1:n.*313A>T
XR_001750194.1:n.5962A>T
XR_001750195.1:n.5605A>T
NM_001308120.2:c.*313A>T MANE Select	NP_001295049.1:n.*313A>T
NM_015091.4:c.*313A>T	NP_055906.2:n.*313A>T
NR_131765.2:n.5698A>T