Canonical Allele Identifier: CA2123856062
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24262002G= , CM000676.2:g.24262002G= GRCh38
NC_000014.8:g.24731208G= , CM000676.1:g.24731208G= GRCh37
NC_000014.7:g.23801048G= NCBI36
NG_007150.1:g.6165C=
NG_007150.2:g.6165C=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.319+32C= MANE Select ENSP00000206765.6:n.319+32C=
ENST00000206765.10:c.319+32C= ENSP00000206765.6:n.319+32C=
ENST00000544573.5:c.-29+125C= ENSP00000439446.1:n.-29+125C=
ENST00000558074.1:c.319+32C= ENSP00000453840.1:n.319+32C=
NM_000359.2:c.319+32C= NP_000350.1:n.319+32C=
NM_000359.3:c.319+32C= MANE Select NP_000350.1:n.319+32C=
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