Canonical Allele Identifier: CA2624689731
Gene: TOGARAM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073773C>A , CM000676.2:g.45073773C>A GRCh38
NC_000014.8:g.45542976C>A , CM000676.1:g.45542976C>A GRCh37
NC_000014.7:g.44612726C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361462.7:c.*212C>A MANE Select ENSP00000354917.2:n.*212C>A
ENST00000361462.6:c.*212C>A ENSP00000354917.2:n.*212C>A
ENST00000361577.7:c.*212C>A ENSP00000355045.3:n.*212C>A
ENST00000556823.1:c.680C>A ENSP00000450465.1:n.680C>A
ENST00000557423.5:c.*2377C>A ENSP00000451829.1:n.*2377C>A
NM_001308120.1:c.*212C>A NP_001295049.1:n.*212C>A
NM_015091.2:c.*212C>A NP_055906.2:n.*212C>A
NM_015091.3:c.*212C>A NP_055906.2:n.*212C>A
NR_131765.1:n.5597C>A
XM_011536571.1:c.*517C>A XP_011534873.1:n.*517C>A
XM_017021098.1:c.*212C>A XP_016876587.1:n.*212C>A
XM_017021099.1:c.*212C>A XP_016876588.1:n.*212C>A
XR_001750194.1:n.5861C>A
XR_001750195.1:n.5504C>A
NM_001308120.2:c.*212C>A MANE Select NP_001295049.1:n.*212C>A
NM_015091.4:c.*212C>A NP_055906.2:n.*212C>A
NR_131765.2:n.5597C>A