Canonical Allele Identifier: CA362832116
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs1142345

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130687T>A , CM000668.2:g.18130687T>A GRCh38
NC_000006.11:g.18130918T>A , CM000668.1:g.18130918T>A GRCh37
NC_000006.10:g.18238897T>A NCBI36
NG_012137.2:g.29457A>T
NG_012137.3:g.29457A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.719A>T MANE Select ENSP00000312304.4:p.Tyr240Phe
ENST00000309983.4:c.719A>T ENSP00000312304.4:p.Tyr240Phe
NM_000367.3:c.719A>T NP_000358.1:p.Tyr240Phe
XM_011514839.1:c.674A>T XP_011513141.1:p.Tyr225Phe
XM_011514840.1:c.650A>T XP_011513142.1:p.Tyr217Phe
NM_000367.4:c.719A>T NP_000358.1:p.Tyr240Phe
NM_001346817.1:c.719A>T NP_001333746.1:p.Tyr240Phe
NM_001346818.1:c.674A>T NP_001333747.1:p.Tyr225Phe
NM_000367.5:c.719A>T MANE Select NP_000358.1:p.Tyr240Phe