Canonical Allele Identifier: CA1086467174
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130529_18130537del , CM000668.2:g.18130529_18130537del GRCh38
NC_000006.11:g.18130760_18130768del , CM000668.1:g.18130760_18130768del GRCh37
NC_000006.10:g.18238739_18238747del NCBI36
NG_012137.2:g.29607_29615del
NG_012137.3:g.29607_29615del

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*131_*139del MANE Select ENSP00000312304.4:n.*131_*139del
ENST00000309983.4:c.*131_*139del ENSP00000312304.4:n.*131_*139del
NM_000367.3:c.*131_*139del NP_000358.1:n.*131_*139del
XM_011514839.1:c.*131_*139del XP_011513141.1:n.*131_*139del
XM_011514840.1:c.*131_*139del XP_011513142.1:n.*131_*139del
NM_000367.4:c.*131_*139del NP_000358.1:n.*131_*139del
NM_001346817.1:c.*131_*139del NP_001333746.1:n.*131_*139del
NM_001346818.1:c.*131_*139del NP_001333747.1:n.*131_*139del
NM_000367.5:c.*131_*139del MANE Select NP_000358.1:n.*131_*139del