Canonical Allele Identifier: CA2123854558
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259081T= , CM000676.2:g.24259081T= GRCh38
NC_000014.8:g.24728287T= , CM000676.1:g.24728287T= GRCh37
NC_000014.7:g.23798127T= NCBI36
NG_007150.1:g.9086A=
NG_007150.2:g.9086A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1153A= MANE Select ENSP00000206765.6:p.Thr385=
ENST00000206765.10:c.1153A= ENSP00000206765.6:p.Thr385=
ENST00000544573.5:c.-28-693A= ENSP00000439446.1:n.-28-693A=
ENST00000559136.1:c.226A= ENSP00000453337.1:p.Thr76=
NM_000359.2:c.1153A= NP_000350.1:p.Thr385=
NM_000359.3:c.1153A= MANE Select NP_000350.1:p.Thr385=
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