Canonical Allele Identifier: CA2123854783
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259538G= , CM000676.2:g.24259538G= GRCh38
NC_000014.8:g.24728744G= , CM000676.1:g.24728744G= GRCh37
NC_000014.7:g.23798584G= NCBI36
NG_007150.1:g.8629C=
NG_007150.2:g.8629C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.984+166C= MANE Select ENSP00000206765.6:n.984+166C=
ENST00000206765.10:c.984+166C= ENSP00000206765.6:n.984+166C=
ENST00000544573.5:c.-28-1150C= ENSP00000439446.1:n.-28-1150C=
ENST00000559136.1:c.57+166C= ENSP00000453337.1:n.57+166C=
NM_000359.2:c.984+166C= NP_000350.1:n.984+166C=
NM_000359.3:c.984+166C= MANE Select NP_000350.1:n.984+166C=
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