Canonical Allele Identifier: CA2123836261
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24258244G= , CM000676.2:g.24258244G= GRCh38
NC_000014.8:g.24727450G= , CM000676.1:g.24727450G= GRCh37
NC_000014.7:g.23797290G= NCBI36
NG_007150.1:g.9923C=
NG_007150.2:g.9923C=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.1402+41C= MANE Select ENSP00000206765.6:n.1402+41C=
ENST00000206765.10:c.1402+41C= ENSP00000206765.6:n.1402+41C=
ENST00000544573.5:c.76+41C= ENSP00000439446.1:n.76+41C=
ENST00000559136.1:c.475+41C= ENSP00000453337.1:n.475+41C=
NM_000359.2:c.1402+41C= NP_000350.1:n.1402+41C=
NM_000359.3:c.1402+41C= MANE Select NP_000350.1:n.1402+41C=
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