Canonical Allele Identifier: CA2123854493
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24258938A= , CM000676.2:g.24258938A= GRCh38
NC_000014.8:g.24728144A= , CM000676.1:g.24728144A= GRCh37
NC_000014.7:g.23797984A= NCBI36
NG_007150.1:g.9229T=
NG_007150.2:g.9229T=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.1159+137T= MANE Select ENSP00000206765.6:n.1159+137T=
ENST00000206765.10:c.1159+137T= ENSP00000206765.6:n.1159+137T=
ENST00000544573.5:c.-28-550T= ENSP00000439446.1:n.-28-550T=
ENST00000559136.1:c.232+137T= ENSP00000453337.1:n.232+137T=
NM_000359.2:c.1159+137T= NP_000350.1:n.1159+137T=
NM_000359.3:c.1159+137T= MANE Select NP_000350.1:n.1159+137T=