Canonical Allele Identifier: CA389264672
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259162T>A , CM000676.2:g.24259162T>A GRCh38
NC_000014.8:g.24728368T>A , CM000676.1:g.24728368T>A GRCh37
NC_000014.7:g.23798208T>A NCBI36
NG_007150.1:g.9005A>T
NG_007150.2:g.9005A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1072A>T MANE Select ENSP00000206765.6:p.Ser358Cys
ENST00000206765.10:c.1072A>T ENSP00000206765.6:p.Ser358Cys
ENST00000544573.5:c.-28-774A>T ENSP00000439446.1:n.-28-774A>T
ENST00000559136.1:c.145A>T ENSP00000453337.1:p.Ser49Cys
NM_000359.2:c.1072A>T NP_000350.1:p.Ser358Cys
NM_000359.3:c.1072A>T MANE Select NP_000350.1:p.Ser358Cys