Canonical Allele Identifier: CA2624346552
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259568_24259569insA , CM000676.2:g.24259568_24259569insA GRCh38
NC_000014.8:g.24728774_24728775insA , CM000676.1:g.24728774_24728775insA GRCh37
NC_000014.7:g.23798614_23798615insA NCBI36
NG_007150.1:g.8598_8599insT
NG_007150.2:g.8598_8599insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.984+135_984+136insT MANE Select ENSP00000206765.6:n.984+135_984+136insT
ENST00000206765.10:c.984+135_984+136insT ENSP00000206765.6:n.984+135_984+136insT
ENST00000544573.5:c.-28-1181_-28-1180insT ENSP00000439446.1:n.-28-1181_-28-1180insT
ENST00000559136.1:c.57+135_57+136insT ENSP00000453337.1:n.57+135_57+136insT
NM_000359.2:c.984+135_984+136insT NP_000350.1:n.984+135_984+136insT
NM_000359.3:c.984+135_984+136insT MANE Select NP_000350.1:n.984+135_984+136insT