Canonical Allele Identifier: CA389265098
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259201C>G , CM000676.2:g.24259201C>G GRCh38
NC_000014.8:g.24728407C>G , CM000676.1:g.24728407C>G GRCh37
NC_000014.7:g.23798247C>G NCBI36
NG_007150.1:g.8966G>C
NG_007150.2:g.8966G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1033G>C MANE Select ENSP00000206765.6:p.Asp345His
ENST00000206765.10:c.1033G>C ENSP00000206765.6:p.Asp345His
ENST00000544573.5:c.-28-813G>C ENSP00000439446.1:n.-28-813G>C
ENST00000559136.1:c.106G>C ENSP00000453337.1:p.Asp36His
NM_000359.2:c.1033G>C NP_000350.1:p.Asp345His
NM_000359.3:c.1033G>C MANE Select NP_000350.1:p.Asp345His