Canonical Allele Identifier: CA389277995
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261785T>G , CM000676.2:g.24261785T>G GRCh38
NC_000014.8:g.24730991T>G , CM000676.1:g.24730991T>G GRCh37
NC_000014.7:g.23800831T>G NCBI36
NG_007150.1:g.6382A>C
NG_007150.2:g.6382A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.418A>C MANE Select ENSP00000206765.6:p.Ile140Leu
ENST00000206765.10:c.418A>C ENSP00000206765.6:p.Ile140Leu
ENST00000544573.5:c.-29+342A>C ENSP00000439446.1:n.-29+342A>C
NM_000359.2:c.418A>C NP_000350.1:p.Ile140Leu
NM_000359.3:c.418A>C MANE Select NP_000350.1:p.Ile140Leu