Canonical Allele Identifier: CA2123855969
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261837C= , CM000676.2:g.24261837C= GRCh38
NC_000014.8:g.24731043C= , CM000676.1:g.24731043C= GRCh37
NC_000014.7:g.23800883C= NCBI36
NG_007150.1:g.6330G=
NG_007150.2:g.6330G=

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.366G= MANE Select ENSP00000206765.6:p.Ser122=
ENST00000206765.10:c.366G= ENSP00000206765.6:p.Ser122=
ENST00000544573.5:c.-29+290G= ENSP00000439446.1:n.-29+290G=
ENST00000558074.1:c.366G= ENSP00000453840.1:p.Ser122=
NM_000359.2:c.366G= NP_000350.1:p.Ser122=
NM_000359.3:c.366G= MANE Select NP_000350.1:p.Ser122=