Canonical Allele Identifier: CA2123836248
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24258239G= , CM000676.2:g.24258239G= GRCh38
NC_000014.8:g.24727445G= , CM000676.1:g.24727445G= GRCh37
NC_000014.7:g.23797285G= NCBI36
NG_007150.1:g.9928C=
NG_007150.2:g.9928C=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.1402+46C= MANE Select ENSP00000206765.6:n.1402+46C=
ENST00000206765.10:c.1402+46C= ENSP00000206765.6:n.1402+46C=
ENST00000544573.5:c.76+46C= ENSP00000439446.1:n.76+46C=
ENST00000559136.1:c.475+46C= ENSP00000453337.1:n.475+46C=
NM_000359.2:c.1402+46C= NP_000350.1:n.1402+46C=
NM_000359.3:c.1402+46C= MANE Select NP_000350.1:n.1402+46C=