Canonical Allele Identifier: CA2123854606
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259197T= , CM000676.2:g.24259197T= GRCh38
NC_000014.8:g.24728403T= , CM000676.1:g.24728403T= GRCh37
NC_000014.7:g.23798243T= NCBI36
NG_007150.1:g.8970A=
NG_007150.2:g.8970A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1037A= MANE Select ENSP00000206765.6:p.Tyr346=
ENST00000206765.10:c.1037A= ENSP00000206765.6:p.Tyr346=
ENST00000544573.5:c.-28-809A= ENSP00000439446.1:n.-28-809A=
ENST00000559136.1:c.110A= ENSP00000453337.1:p.Tyr37=
NM_000359.2:c.1037A= NP_000350.1:p.Tyr346=
NM_000359.3:c.1037A= MANE Select NP_000350.1:p.Tyr346=