Canonical Allele Identifier: CA2677457387
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130565dup , CM000668.2:g.18130565dup GRCh38
NC_000006.11:g.18130796dup , CM000668.1:g.18130796dup GRCh37
NC_000006.10:g.18238775dup NCBI36
NG_012137.2:g.29581dup
NG_012137.3:g.29581dup

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*105dup MANE Select ENSP00000312304.4:n.*105dup
ENST00000309983.4:c.*105dup ENSP00000312304.4:n.*105dup
NM_000367.3:c.*105dup NP_000358.1:n.*105dup
XM_011514839.1:c.*105dup XP_011513141.1:n.*105dup
XM_011514840.1:c.*105dup XP_011513142.1:n.*105dup
NM_000367.4:c.*105dup NP_000358.1:n.*105dup
NM_001346817.1:c.*105dup NP_001333746.1:n.*105dup
NM_001346818.1:c.*105dup NP_001333747.1:n.*105dup
NM_000367.5:c.*105dup MANE Select NP_000358.1:n.*105dup