Canonical Allele Identifier: CA2123854586
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259153T= , CM000676.2:g.24259153T= GRCh38
NC_000014.8:g.24728359T= , CM000676.1:g.24728359T= GRCh37
NC_000014.7:g.23798199T= NCBI36
NG_007150.1:g.9014A=
NG_007150.2:g.9014A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1081A= MANE Select ENSP00000206765.6:p.Ile361=
ENST00000206765.10:c.1081A= ENSP00000206765.6:p.Ile361=
ENST00000544573.5:c.-28-765A= ENSP00000439446.1:n.-28-765A=
ENST00000559136.1:c.154A= ENSP00000453337.1:p.Ile52=
NM_000359.2:c.1081A= NP_000350.1:p.Ile361=
NM_000359.3:c.1081A= MANE Select NP_000350.1:p.Ile361=