Canonical Allele Identifier: CA2123854777
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259529_24259530delinsTG , CM000676.2:g.24259529_24259530delinsTG GRCh38
NC_000014.8:g.24728735_24728736delinsTG , CM000676.1:g.24728735_24728736delinsTG GRCh37
NC_000014.7:g.23798575_23798576delinsTG NCBI36
NG_007150.1:g.8637_8638delinsCA
NG_007150.2:g.8637_8638delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.984+174_984+175delinsCA MANE Select ENSP00000206765.6:n.984+174_984+175delinsCA
ENST00000206765.10:c.984+174_984+175delinsCA ENSP00000206765.6:n.984+174_984+175delinsCA
ENST00000544573.5:c.-28-1142_-28-1141delinsCA ENSP00000439446.1:n.-28-1142_-28-1141delinsCA
ENST00000559136.1:c.57+174_57+175delinsCA ENSP00000453337.1:n.57+174_57+175delinsCA
NM_000359.2:c.984+174_984+175delinsCA NP_000350.1:n.984+174_984+175delinsCA
NM_000359.3:c.984+174_984+175delinsCA MANE Select NP_000350.1:n.984+174_984+175delinsCA