Canonical Allele Identifier: CA2123854747
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259465T= , CM000676.2:g.24259465T= GRCh38
NC_000014.8:g.24728671T= , CM000676.1:g.24728671T= GRCh37
NC_000014.7:g.23798511T= NCBI36
NG_007150.1:g.8702A=
NG_007150.2:g.8702A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.985-216A= MANE Select ENSP00000206765.6:n.985-216A=
ENST00000206765.10:c.985-216A= ENSP00000206765.6:n.985-216A=
ENST00000544573.5:c.-28-1077A= ENSP00000439446.1:n.-28-1077A=
ENST00000559136.1:c.58-216A= ENSP00000453337.1:n.58-216A=
NM_000359.2:c.985-216A= NP_000350.1:n.985-216A=
NM_000359.3:c.985-216A= MANE Select NP_000350.1:n.985-216A=
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