Canonical Allele Identifier: CA1086467180
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130541_18130556del , CM000668.2:g.18130541_18130556del GRCh38
NC_000006.11:g.18130772_18130787del , CM000668.1:g.18130772_18130787del GRCh37
NC_000006.10:g.18238751_18238766del NCBI36
NG_012137.2:g.29588_29603del
NG_012137.3:g.29588_29603del

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*112_*127del MANE Select ENSP00000312304.4:n.*112_*127del
ENST00000309983.4:c.*112_*127del ENSP00000312304.4:n.*112_*127del
NM_000367.3:c.*112_*127del NP_000358.1:n.*112_*127del
XM_011514839.1:c.*112_*127del XP_011513141.1:n.*112_*127del
XM_011514840.1:c.*112_*127del XP_011513142.1:n.*112_*127del
NM_000367.4:c.*112_*127del NP_000358.1:n.*112_*127del
NM_001346817.1:c.*112_*127del NP_001333746.1:n.*112_*127del
NM_001346818.1:c.*112_*127del NP_001333747.1:n.*112_*127del
NM_000367.5:c.*112_*127del MANE Select NP_000358.1:n.*112_*127del