Canonical Allele Identifier: CA389264382
Gene: TGM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.24728355A>C (hg19) chr14:g.24259149A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259149A>C , CM000676.2:g.24259149A>C GRCh38
NC_000014.8:g.24728355A>C , CM000676.1:g.24728355A>C GRCh37
NC_000014.7:g.23798195A>C NCBI36
NG_007150.1:g.9018T>G
NG_007150.2:g.9018T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1085T>G MANE Select ENSP00000206765.6:p.Leu362Arg
ENST00000206765.10:c.1085T>G ENSP00000206765.6:p.Leu362Arg
ENST00000544573.5:c.-28-761T>G ENSP00000439446.1:n.-28-761T>G
ENST00000559136.1:c.158T>G ENSP00000453337.1:p.Leu53Arg
NM_000359.2:c.1085T>G NP_000350.1:p.Leu362Arg
NM_000359.3:c.1085T>G MANE Select NP_000350.1:p.Leu362Arg
Search 100 bp 5'
Search 100 bp 3'