Canonical Allele Identifier: CA362832062
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130669T>A , CM000668.2:g.18130669T>A GRCh38
NC_000006.11:g.18130900T>A , CM000668.1:g.18130900T>A GRCh37
NC_000006.10:g.18238879T>A NCBI36
NG_012137.2:g.29475A>T
NG_012137.3:g.29475A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.737A>T MANE Select ENSP00000312304.4:p.Ter246Leu
ENST00000309983.4:c.737A>T ENSP00000312304.4:p.Ter246Leu
NM_000367.3:c.737A>T NP_000358.1:p.Ter246Leu
XM_011514839.1:c.692A>T XP_011513141.1:p.Ter231Leu
XM_011514840.1:c.668A>T XP_011513142.1:p.Ter223Leu
NM_000367.4:c.737A>T NP_000358.1:p.Ter246Leu
NM_001346817.1:c.737A>T NP_001333746.1:p.Ter246Leu
NM_001346818.1:c.692A>T NP_001333747.1:p.Ter231Leu
NM_000367.5:c.737A>T MANE Select NP_000358.1:p.Ter246Leu