Canonical Allele Identifier: CA389264652

Gene: TGM1

Linked Data

• MyVariant Identifiers: chr14:g.24728367C>A (hg19) ; chr14:g.24259161C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24259161C>A , CM000676.2:g.24259161C>A	GRCh38
NC_000014.8:g.24728367C>A , CM000676.1:g.24728367C>A	GRCh37
NC_000014.7:g.23798207C>A	NCBI36
NG_007150.1:g.9006G>T
NG_007150.2:g.9006G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206765.11:c.1073G>T MANE Select	ENSP00000206765.6:p.Ser358Ile
ENST00000206765.10:c.1073G>T	ENSP00000206765.6:p.Ser358Ile
ENST00000544573.5:c.-28-773G>T	ENSP00000439446.1:n.-28-773G>T
ENST00000559136.1:c.146G>T	ENSP00000453337.1:p.Ser49Ile
NM_000359.2:c.1073G>T	NP_000350.1:p.Ser358Ile
NM_000359.3:c.1073G>T MANE Select	NP_000350.1:p.Ser358Ile