Canonical Allele Identifier: CA389276860
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261703A>C , CM000676.2:g.24261703A>C GRCh38
NC_000014.8:g.24730909A>C , CM000676.1:g.24730909A>C GRCh37
NC_000014.7:g.23800749A>C NCBI36
NG_007150.1:g.6464T>G
NG_007150.2:g.6464T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.500T>G MANE Select ENSP00000206765.6:p.Leu167Ter
ENST00000206765.10:c.500T>G ENSP00000206765.6:p.Leu167Ter
ENST00000544573.5:c.-29+424T>G ENSP00000439446.1:n.-29+424T>G
NM_000359.2:c.500T>G NP_000350.1:p.Leu167Ter
NM_000359.3:c.500T>G MANE Select NP_000350.1:p.Leu167Ter