Canonical Allele Identifier: CA2123836231
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24258234A= , CM000676.2:g.24258234A= GRCh38
NC_000014.8:g.24727440A= , CM000676.1:g.24727440A= GRCh37
NC_000014.7:g.23797280A= NCBI36
NG_007150.1:g.9933T=
NG_007150.2:g.9933T=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.1402+51T= MANE Select ENSP00000206765.6:n.1402+51T=
ENST00000206765.10:c.1402+51T= ENSP00000206765.6:n.1402+51T=
ENST00000544573.5:c.76+51T= ENSP00000439446.1:n.76+51T=
ENST00000559136.1:c.475+51T= ENSP00000453337.1:n.475+51T=
NM_000359.2:c.1402+51T= NP_000350.1:n.1402+51T=
NM_000359.3:c.1402+51T= MANE Select NP_000350.1:n.1402+51T=