Canonical Allele Identifier: CA2123854589
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259160G= , CM000676.2:g.24259160G= GRCh38
NC_000014.8:g.24728366G= , CM000676.1:g.24728366G= GRCh37
NC_000014.7:g.23798206G= NCBI36
NG_007150.1:g.9007C=
NG_007150.2:g.9007C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1074C= MANE Select ENSP00000206765.6:p.Ser358=
ENST00000206765.10:c.1074C= ENSP00000206765.6:p.Ser358=
ENST00000544573.5:c.-28-772C= ENSP00000439446.1:n.-28-772C=
ENST00000559136.1:c.147C= ENSP00000453337.1:p.Ser49=
NM_000359.2:c.1074C= NP_000350.1:p.Ser358=
NM_000359.3:c.1074C= MANE Select NP_000350.1:p.Ser358=