Canonical Allele Identifier: CA2123831939
Gene: TGM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24255826T= , CM000676.2:g.24255826T= GRCh38
NC_000014.8:g.24725032T= , CM000676.1:g.24725032T= GRCh37
NC_000014.7:g.23794872T= NCBI36
NG_007150.1:g.12341A=
NG_007150.2:g.12341A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1491+163A= MANE Select ENSP00000206765.6:n.1491+163A=
ENST00000206765.10:c.1491+163A= ENSP00000206765.6:n.1491+163A=
ENST00000544573.5:c.165+163A= ENSP00000439446.1:n.165+163A=
ENST00000559136.1:c.564+163A= ENSP00000453337.1:n.564+163A=
NM_000359.2:c.1491+163A= NP_000350.1:n.1491+163A=
NM_000359.3:c.1491+163A= MANE Select NP_000350.1:n.1491+163A=
Search 100 bp 5'
Search 100 bp 3'