Canonical Allele Identifier: CA362832087
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130678G>T , CM000668.2:g.18130678G>T GRCh38
NC_000006.11:g.18130909G>T , CM000668.1:g.18130909G>T GRCh37
NC_000006.10:g.18238888G>T NCBI36
NG_012137.2:g.29466C>A
NG_012137.3:g.29466C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.728C>A MANE Select ENSP00000312304.4:p.Thr243Lys
ENST00000309983.4:c.728C>A ENSP00000312304.4:p.Thr243Lys
NM_000367.3:c.728C>A NP_000358.1:p.Thr243Lys
XM_011514839.1:c.683C>A XP_011513141.1:p.Thr228Lys
XM_011514840.1:c.659C>A XP_011513142.1:p.Thr220Lys
NM_000367.4:c.728C>A NP_000358.1:p.Thr243Lys
NM_001346817.1:c.728C>A NP_001333746.1:p.Thr243Lys
NM_001346818.1:c.683C>A NP_001333747.1:p.Thr228Lys
NM_000367.5:c.728C>A MANE Select NP_000358.1:p.Thr243Lys