Canonical Allele Identifier: CA389276941
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261707C>G , CM000676.2:g.24261707C>G GRCh38
NC_000014.8:g.24730913C>G , CM000676.1:g.24730913C>G GRCh37
NC_000014.7:g.23800753C>G NCBI36
NG_007150.1:g.6460G>C
NG_007150.2:g.6460G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.496G>C MANE Select ENSP00000206765.6:p.Glu166Gln
ENST00000206765.10:c.496G>C ENSP00000206765.6:p.Glu166Gln
ENST00000544573.5:c.-29+420G>C ENSP00000439446.1:n.-29+420G>C
NM_000359.2:c.496G>C NP_000350.1:p.Glu166Gln
NM_000359.3:c.496G>C MANE Select NP_000350.1:p.Glu166Gln