Canonical Allele Identifier: CA362835719
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18139029A>C , CM000668.2:g.18139029A>C GRCh38
NC_000006.11:g.18139260A>C , CM000668.1:g.18139260A>C GRCh37
NC_000006.10:g.18247239A>C NCBI36
NG_012137.2:g.21115T>G
NG_012137.3:g.21115T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.428T>G MANE Select ENSP00000312304.4:p.Ile143Ser
ENST00000309983.4:c.428T>G ENSP00000312304.4:p.Ile143Ser
NM_000367.3:c.428T>G NP_000358.1:p.Ile143Ser
XM_011514839.1:c.428T>G XP_011513141.1:p.Ile143Ser
XM_011514840.1:c.359T>G XP_011513142.1:p.Ile120Ser
NM_000367.4:c.428T>G NP_000358.1:p.Ile143Ser
NM_001346817.1:c.428T>G NP_001333746.1:p.Ile143Ser
NM_001346818.1:c.428T>G NP_001333747.1:p.Ile143Ser
NM_000367.5:c.428T>G MANE Select NP_000358.1:p.Ile143Ser