Canonical Allele Identifier: CA2123854800
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259581T= , CM000676.2:g.24259581T= GRCh38
NC_000014.8:g.24728787T= , CM000676.1:g.24728787T= GRCh37
NC_000014.7:g.23798627T= NCBI36
NG_007150.1:g.8586A=
NG_007150.2:g.8586A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.984+123A= MANE Select ENSP00000206765.6:n.984+123A=
ENST00000206765.10:c.984+123A= ENSP00000206765.6:n.984+123A=
ENST00000544573.5:c.-28-1193A= ENSP00000439446.1:n.-28-1193A=
ENST00000559136.1:c.57+123A= ENSP00000453337.1:n.57+123A=
NM_000359.2:c.984+123A= NP_000350.1:n.984+123A=
NM_000359.3:c.984+123A= MANE Select NP_000350.1:n.984+123A=