Canonical Allele Identifier: CA2123854730
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259435_24259437delinsGCT , CM000676.2:g.24259435_24259437delinsGCT GRCh38
NC_000014.8:g.24728641_24728643delinsGCT , CM000676.1:g.24728641_24728643delinsGCT GRCh37
NC_000014.7:g.23798481_23798483delinsGCT NCBI36
NG_007150.1:g.8730_8732delinsAGC
NG_007150.2:g.8730_8732delinsAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.985-188_985-186delinsAGC MANE Select ENSP00000206765.6:n.985-188_985-186delinsAGC
ENST00000206765.10:c.985-188_985-186delinsAGC ENSP00000206765.6:n.985-188_985-186delinsAGC
ENST00000544573.5:c.-28-1049_-28-1047delinsAGC ENSP00000439446.1:n.-28-1049_-28-1047delinsAGC
ENST00000559136.1:c.58-188_58-186delinsAGC ENSP00000453337.1:n.58-188_58-186delinsAGC
NM_000359.2:c.985-188_985-186delinsAGC NP_000350.1:n.985-188_985-186delinsAGC
NM_000359.3:c.985-188_985-186delinsAGC MANE Select NP_000350.1:n.985-188_985-186delinsAGC