Canonical Allele Identifier: CA2578538780
Gene: TPMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130681del , CM000668.2:g.18130681del GRCh38
NC_000006.11:g.18130912del , CM000668.1:g.18130912del GRCh37
NC_000006.10:g.18238891del NCBI36
NG_012137.2:g.29464del
NG_012137.3:g.29464del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.726del MANE Select ENSP00000312304.4:p.Thr243GlnfsTer5
ENST00000309983.4:c.726del ENSP00000312304.4:p.Thr243GlnfsTer5
NM_000367.3:c.726del NP_000358.1:p.Thr243GlnfsTer5
XM_011514839.1:c.681del XP_011513141.1:p.Thr228GlnfsTer5
XM_011514840.1:c.657del XP_011513142.1:p.Thr220GlnfsTer5
NM_000367.4:c.726del NP_000358.1:p.Thr243GlnfsTer5
NM_001346817.1:c.726del NP_001333746.1:p.Thr243GlnfsTer5
NM_001346818.1:c.681del NP_001333747.1:p.Thr228GlnfsTer5
NM_000367.5:c.726del MANE Select NP_000358.1:p.Thr243GlnfsTer5