Canonical Allele Identifier: CA485664018
Gene: TGM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.24728426C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259220C>G , CM000676.2:g.24259220C>G GRCh38
NC_000014.8:g.24728426C>G , CM000676.1:g.24728426C>G GRCh37
NC_000014.7:g.23798266C>G NCBI36
NG_007150.1:g.8947G>C
NG_007150.2:g.8947G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1014G>C MANE Select ENSP00000206765.6:p.Leu338=
ENST00000206765.10:c.1014G>C ENSP00000206765.6:p.Leu338=
ENST00000544573.5:c.-28-832G>C ENSP00000439446.1:n.-28-832G>C
ENST00000559136.1:c.87G>C ENSP00000453337.1:p.Leu29=
NM_000359.2:c.1014G>C NP_000350.1:p.Leu338=
NM_000359.3:c.1014G>C MANE Select NP_000350.1:p.Leu338=
Search 100 bp 5'
Search 100 bp 3'