Canonical Allele Identifier: CA645551455
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130702del , CM000668.2:g.18130702del GRCh38
NC_000006.11:g.18130933del , CM000668.1:g.18130933del GRCh37
NC_000006.10:g.18238912del NCBI36
NG_012137.2:g.29446del
NG_012137.3:g.29446del

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.708del MANE Select ENSP00000312304.4:p.Phe236LeufsTer12
ENST00000309983.4:c.708del ENSP00000312304.4:p.Phe236LeufsTer12
NM_000367.3:c.708del NP_000358.1:p.Phe236LeufsTer12
XM_011514839.1:c.663del XP_011513141.1:p.Phe221LeufsTer12
XM_011514840.1:c.639del XP_011513142.1:p.Phe213LeufsTer12
NM_000367.4:c.708del NP_000358.1:p.Phe236LeufsTer12
NM_001346817.1:c.708del NP_001333746.1:p.Phe236LeufsTer12
NM_001346818.1:c.663del NP_001333747.1:p.Phe221LeufsTer12
NM_000367.5:c.708del MANE Select NP_000358.1:p.Phe236LeufsTer12