Canonical Allele Identifier: CA389276822
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261701G>T , CM000676.2:g.24261701G>T GRCh38
NC_000014.8:g.24730907G>T , CM000676.1:g.24730907G>T GRCh37
NC_000014.7:g.23800747G>T NCBI36
NG_007150.1:g.6466C>A
NG_007150.2:g.6466C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.502C>A MANE Select ENSP00000206765.6:p.Leu168Ile
ENST00000206765.10:c.502C>A ENSP00000206765.6:p.Leu168Ile
ENST00000544573.5:c.-29+426C>A ENSP00000439446.1:n.-29+426C>A
NM_000359.2:c.502C>A NP_000350.1:p.Leu168Ile
NM_000359.3:c.502C>A MANE Select NP_000350.1:p.Leu168Ile