Canonical Allele Identifier: CA389256162
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24256026A>C , CM000676.2:g.24256026A>C GRCh38
NC_000014.8:g.24725232A>C , CM000676.1:g.24725232A>C GRCh37
NC_000014.7:g.23795072A>C NCBI36
NG_007150.1:g.12141T>G
NG_007150.2:g.12141T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1454T>G MANE Select ENSP00000206765.6:p.Val485Gly
ENST00000206765.10:c.1454T>G ENSP00000206765.6:p.Val485Gly
ENST00000544573.5:c.128T>G ENSP00000439446.1:p.Val43Gly
ENST00000559136.1:c.527T>G ENSP00000453337.1:p.Val176Gly
NM_000359.2:c.1454T>G NP_000350.1:p.Val485Gly
NM_000359.3:c.1454T>G MANE Select NP_000350.1:p.Val485Gly