Canonical Allele Identifier: CA2123854767
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259508C= , CM000676.2:g.24259508C= GRCh38
NC_000014.8:g.24728714C= , CM000676.1:g.24728714C= GRCh37
NC_000014.7:g.23798554C= NCBI36
NG_007150.1:g.8659G=
NG_007150.2:g.8659G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.984+196G= MANE Select ENSP00000206765.6:n.984+196G=
ENST00000206765.10:c.984+196G= ENSP00000206765.6:n.984+196G=
ENST00000544573.5:c.-28-1120G= ENSP00000439446.1:n.-28-1120G=
ENST00000559136.1:c.57+196G= ENSP00000453337.1:n.57+196G=
NM_000359.2:c.984+196G= NP_000350.1:n.984+196G=
NM_000359.3:c.984+196G= MANE Select NP_000350.1:n.984+196G=