Canonical Allele Identifier: CA2123832286
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24255970C= , CM000676.2:g.24255970C= GRCh38
NC_000014.8:g.24725176C= , CM000676.1:g.24725176C= GRCh37
NC_000014.7:g.23795016C= NCBI36
NG_007150.1:g.12197G=
NG_007150.2:g.12197G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1491+19G= MANE Select ENSP00000206765.6:n.1491+19G=
ENST00000206765.10:c.1491+19G= ENSP00000206765.6:n.1491+19G=
ENST00000544573.5:c.165+19G= ENSP00000439446.1:n.165+19G=
ENST00000559136.1:c.564+19G= ENSP00000453337.1:n.564+19G=
NM_000359.2:c.1491+19G= NP_000350.1:n.1491+19G=
NM_000359.3:c.1491+19G= MANE Select NP_000350.1:n.1491+19G=