Canonical Allele Identifier: CA2123854557
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259079G= , CM000676.2:g.24259079G= GRCh38
NC_000014.8:g.24728285G= , CM000676.1:g.24728285G= GRCh37
NC_000014.7:g.23798125G= NCBI36
NG_007150.1:g.9088C=
NG_007150.2:g.9088C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1155C= MANE Select ENSP00000206765.6:p.Thr385=
ENST00000206765.10:c.1155C= ENSP00000206765.6:p.Thr385=
ENST00000544573.5:c.-28-691C= ENSP00000439446.1:n.-28-691C=
ENST00000559136.1:c.228C= ENSP00000453337.1:p.Thr76=
NM_000359.2:c.1155C= NP_000350.1:p.Thr385=
NM_000359.3:c.1155C= MANE Select NP_000350.1:p.Thr385=
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