Canonical Allele Identifier: CA961133441
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259648T>G , CM000676.2:g.24259648T>G GRCh38
NC_000014.8:g.24728854T>G , CM000676.1:g.24728854T>G GRCh37
NC_000014.7:g.23798694T>G NCBI36
NG_007150.1:g.8519A>C
NG_007150.2:g.8519A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.984+56A>C MANE Select ENSP00000206765.6:n.984+56A>C
ENST00000206765.10:c.984+56A>C ENSP00000206765.6:n.984+56A>C
ENST00000544573.5:c.-28-1260A>C ENSP00000439446.1:n.-28-1260A>C
ENST00000559136.1:c.57+56A>C ENSP00000453337.1:n.57+56A>C
NM_000359.2:c.984+56A>C NP_000350.1:n.984+56A>C
NM_000359.3:c.984+56A>C MANE Select NP_000350.1:n.984+56A>C