Canonical Allele Identifier: CA389263463
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1299251012
gnomAD v2: 14-24728298-G-C
gnomAD v4: 14-24259092-G-C
MyVariant Identifiers: chr14:g.24728298G>C (hg19) chr14:g.24259092G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259092G>C , CM000676.2:g.24259092G>C GRCh38
NC_000014.8:g.24728298G>C , CM000676.1:g.24728298G>C GRCh37
NC_000014.7:g.23798138G>C NCBI36
NG_007150.1:g.9075C>G
NG_007150.2:g.9075C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1142C>G MANE Select ENSP00000206765.6:p.Ala381Gly
ENST00000206765.10:c.1142C>G ENSP00000206765.6:p.Ala381Gly
ENST00000544573.5:c.-28-704C>G ENSP00000439446.1:n.-28-704C>G
ENST00000559136.1:c.215C>G ENSP00000453337.1:p.Ala72Gly
NM_000359.2:c.1142C>G NP_000350.1:p.Ala381Gly
NM_000359.3:c.1142C>G MANE Select NP_000350.1:p.Ala381Gly
Search 100 bp 5'
Search 100 bp 3'