Canonical Allele Identifier: CA2123854752
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259485C= , CM000676.2:g.24259485C= GRCh38
NC_000014.8:g.24728691C= , CM000676.1:g.24728691C= GRCh37
NC_000014.7:g.23798531C= NCBI36
NG_007150.1:g.8682G=
NG_007150.2:g.8682G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.984+219G= MANE Select ENSP00000206765.6:n.984+219G=
ENST00000206765.10:c.984+219G= ENSP00000206765.6:n.984+219G=
ENST00000544573.5:c.-28-1097G= ENSP00000439446.1:n.-28-1097G=
ENST00000559136.1:c.57+219G= ENSP00000453337.1:n.57+219G=
NM_000359.2:c.984+219G= NP_000350.1:n.984+219G=
NM_000359.3:c.984+219G= MANE Select NP_000350.1:n.984+219G=
Search 100 bp 5'
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