Canonical Allele Identifier: CA2123854592
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259173G= , CM000676.2:g.24259173G= GRCh38
NC_000014.8:g.24728379G= , CM000676.1:g.24728379G= GRCh37
NC_000014.7:g.23798219G= NCBI36
NG_007150.1:g.8994C=
NG_007150.2:g.8994C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1061C= MANE Select ENSP00000206765.6:p.Ala354=
ENST00000206765.10:c.1061C= ENSP00000206765.6:p.Ala354=
ENST00000544573.5:c.-28-785C= ENSP00000439446.1:n.-28-785C=
ENST00000559136.1:c.134C= ENSP00000453337.1:p.Ala45=
NM_000359.2:c.1061C= NP_000350.1:p.Ala354=
NM_000359.3:c.1061C= MANE Select NP_000350.1:p.Ala354=