Canonical Allele Identifier: CA2123855878
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261692G= , CM000676.2:g.24261692G= GRCh38
NC_000014.8:g.24730898G= , CM000676.1:g.24730898G= GRCh37
NC_000014.7:g.23800738G= NCBI36
NG_007150.1:g.6475C=
NG_007150.2:g.6475C=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.508+3C= MANE Select ENSP00000206765.6:n.508+3C=
ENST00000206765.10:c.508+3C= ENSP00000206765.6:n.508+3C=
ENST00000544573.5:c.-29+435C= ENSP00000439446.1:n.-29+435C=
NM_000359.2:c.508+3C= NP_000350.1:n.508+3C=
NM_000359.3:c.508+3C= MANE Select NP_000350.1:n.508+3C=