Canonical Allele Identifier: CA389277989
Gene: TGM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261784A>T , CM000676.2:g.24261784A>T GRCh38
NC_000014.8:g.24730990A>T , CM000676.1:g.24730990A>T GRCh37
NC_000014.7:g.23800830A>T NCBI36
NG_007150.1:g.6383T>A
NG_007150.2:g.6383T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.419T>A MANE Select ENSP00000206765.6:p.Ile140Lys
ENST00000206765.10:c.419T>A ENSP00000206765.6:p.Ile140Lys
ENST00000544573.5:c.-29+343T>A ENSP00000439446.1:n.-29+343T>A
NM_000359.2:c.419T>A NP_000350.1:p.Ile140Lys
NM_000359.3:c.419T>A MANE Select NP_000350.1:p.Ile140Lys