Canonical Allele Identifier: CA485664014

Gene: TGM1

Linked Data

• MyVariant Identifiers: chr14:g.24728423A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24259217A>T , CM000676.2:g.24259217A>T	GRCh38
NC_000014.8:g.24728423A>T , CM000676.1:g.24728423A>T	GRCh37
NC_000014.7:g.23798263A>T	NCBI36
NG_007150.1:g.8950T>A
NG_007150.2:g.8950T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206765.11:c.1017T>A MANE Select	ENSP00000206765.6:p.Ile339=
ENST00000206765.10:c.1017T>A	ENSP00000206765.6:p.Ile339=
ENST00000544573.5:c.-28-829T>A	ENSP00000439446.1:n.-28-829T>A
ENST00000559136.1:c.90T>A	ENSP00000453337.1:p.Ile30=
NM_000359.2:c.1017T>A	NP_000350.1:p.Ile339=
NM_000359.3:c.1017T>A MANE Select	NP_000350.1:p.Ile339=