Canonical Allele Identifier: CA362832835
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130778T>C , CM000668.2:g.18130778T>C GRCh38
NC_000006.11:g.18131009T>C , CM000668.1:g.18131009T>C GRCh37
NC_000006.10:g.18238988T>C NCBI36
NG_012137.2:g.29366A>G
NG_012137.3:g.29366A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.628A>G MANE Select ENSP00000312304.4:p.Lys210Glu
ENST00000309983.4:c.628A>G ENSP00000312304.4:p.Lys210Glu
NM_000367.3:c.628A>G NP_000358.1:p.Lys210Glu
XM_011514839.1:c.583A>G XP_011513141.1:p.Lys195Glu
XM_011514840.1:c.559A>G XP_011513142.1:p.Lys187Glu
NM_000367.4:c.628A>G NP_000358.1:p.Lys210Glu
NM_001346817.1:c.628A>G NP_001333746.1:p.Lys210Glu
NM_001346818.1:c.583A>G NP_001333747.1:p.Lys195Glu
NM_000367.5:c.628A>G MANE Select NP_000358.1:p.Lys210Glu