Canonical Allele Identifier: CA389264392
Gene: TGM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.24728356G>T (hg19) chr14:g.24259150G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259150G>T , CM000676.2:g.24259150G>T GRCh38
NC_000014.8:g.24728356G>T , CM000676.1:g.24728356G>T GRCh37
NC_000014.7:g.23798196G>T NCBI36
NG_007150.1:g.9017C>A
NG_007150.2:g.9017C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1084C>A MANE Select ENSP00000206765.6:p.Leu362Met
ENST00000206765.10:c.1084C>A ENSP00000206765.6:p.Leu362Met
ENST00000544573.5:c.-28-762C>A ENSP00000439446.1:n.-28-762C>A
ENST00000559136.1:c.157C>A ENSP00000453337.1:p.Leu53Met
NM_000359.2:c.1084C>A NP_000350.1:p.Leu362Met
NM_000359.3:c.1084C>A MANE Select NP_000350.1:p.Leu362Met
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Search 100 bp 3'