Canonical Allele Identifier: CA2123832647
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24256080A= , CM000676.2:g.24256080A= GRCh38
NC_000014.8:g.24725286A= , CM000676.1:g.24725286A= GRCh37
NC_000014.7:g.23795126A= NCBI36
NG_007150.1:g.12087T=
NG_007150.2:g.12087T=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.1403-3T= MANE Select ENSP00000206765.6:n.1403-3T=
ENST00000206765.10:c.1403-3T= ENSP00000206765.6:n.1403-3T=
ENST00000544573.5:c.77-3T= ENSP00000439446.1:n.77-3T=
ENST00000559136.1:c.476-3T= ENSP00000453337.1:n.476-3T=
NM_000359.2:c.1403-3T= NP_000350.1:n.1403-3T=
NM_000359.3:c.1403-3T= MANE Select NP_000350.1:n.1403-3T=