Canonical Allele Identifier: CA2624689737
Gene: TOGARAM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073785G>T , CM000676.2:g.45073785G>T GRCh38
NC_000014.8:g.45542988G>T , CM000676.1:g.45542988G>T GRCh37
NC_000014.7:g.44612738G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361462.7:c.*224G>T MANE Select ENSP00000354917.2:n.*224G>T
ENST00000361462.6:c.*224G>T ENSP00000354917.2:n.*224G>T
ENST00000361577.7:c.*224G>T ENSP00000355045.3:n.*224G>T
ENST00000556823.1:c.692G>T ENSP00000450465.1:n.692G>T
ENST00000557423.5:c.*2389G>T ENSP00000451829.1:n.*2389G>T
NM_001308120.1:c.*224G>T NP_001295049.1:n.*224G>T
NM_015091.2:c.*224G>T NP_055906.2:n.*224G>T
NM_015091.3:c.*224G>T NP_055906.2:n.*224G>T
NR_131765.1:n.5609G>T
XM_011536571.1:c.*529G>T XP_011534873.1:n.*529G>T
XM_017021098.1:c.*224G>T XP_016876587.1:n.*224G>T
XM_017021099.1:c.*224G>T XP_016876588.1:n.*224G>T
XR_001750194.1:n.5873G>T
XR_001750195.1:n.5516G>T
NM_001308120.2:c.*224G>T MANE Select NP_001295049.1:n.*224G>T
NM_015091.4:c.*224G>T NP_055906.2:n.*224G>T
NR_131765.2:n.5609G>T