Canonical Allele Identifier: CA362838259
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18143642T>A , CM000668.2:g.18143642T>A GRCh38
NC_000006.11:g.18143873T>A , CM000668.1:g.18143873T>A GRCh37
NC_000006.10:g.18251852T>A NCBI36
NG_012137.2:g.16502A>T
NG_012137.3:g.16502A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.320A>T MANE Select ENSP00000312304.4:p.Tyr107Phe
ENST00000309983.4:c.320A>T ENSP00000312304.4:p.Tyr107Phe
NM_000367.3:c.320A>T NP_000358.1:p.Tyr107Phe
XM_011514839.1:c.320A>T XP_011513141.1:p.Tyr107Phe
XM_011514840.1:c.251A>T XP_011513142.1:p.Tyr84Phe
NM_000367.4:c.320A>T NP_000358.1:p.Tyr107Phe
NM_001346817.1:c.320A>T NP_001333746.1:p.Tyr107Phe
NM_001346818.1:c.320A>T NP_001333747.1:p.Tyr107Phe
NM_000367.5:c.320A>T MANE Select NP_000358.1:p.Tyr107Phe