Canonical Allele Identifier: CA2123854489
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24258926C= , CM000676.2:g.24258926C= GRCh38
NC_000014.8:g.24728132C= , CM000676.1:g.24728132C= GRCh37
NC_000014.7:g.23797972C= NCBI36
NG_007150.1:g.9241G=
NG_007150.2:g.9241G=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.1159+149G= MANE Select ENSP00000206765.6:n.1159+149G=
ENST00000206765.10:c.1159+149G= ENSP00000206765.6:n.1159+149G=
ENST00000544573.5:c.-28-538G= ENSP00000439446.1:n.-28-538G=
ENST00000559136.1:c.232+149G= ENSP00000453337.1:n.232+149G=
NM_000359.2:c.1159+149G= NP_000350.1:n.1159+149G=
NM_000359.3:c.1159+149G= MANE Select NP_000350.1:n.1159+149G=
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