Canonical Allele Identifier: CA1613545671
Gene: TPMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130635T= , CM000668.2:g.18130635T= GRCh38
NC_000006.11:g.18130866T= , CM000668.1:g.18130866T= GRCh37
NC_000006.10:g.18238845T= NCBI36
NG_012137.2:g.29509A=
NG_012137.3:g.29509A=

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*33A= MANE Select ENSP00000312304.4:n.*33A=
ENST00000309983.4:c.*33A= ENSP00000312304.4:n.*33A=
NM_000367.3:c.*33A= NP_000358.1:n.*33A=
XM_011514839.1:c.*33A= XP_011513141.1:n.*33A=
XM_011514840.1:c.*33A= XP_011513142.1:n.*33A=
NM_000367.4:c.*33A= NP_000358.1:n.*33A=
NM_001346817.1:c.*33A= NP_001333746.1:n.*33A=
NM_001346818.1:c.*33A= NP_001333747.1:n.*33A=
NM_000367.5:c.*33A= MANE Select NP_000358.1:n.*33A=