Canonical Allele Identifier: CA362838344
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18143665A>T , CM000668.2:g.18143665A>T GRCh38
NC_000006.11:g.18143896A>T , CM000668.1:g.18143896A>T GRCh37
NC_000006.10:g.18251875A>T NCBI36
NG_012137.2:g.16479T>A
NG_012137.3:g.16479T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.297T>A MANE Select ENSP00000312304.4:p.Phe99Leu
ENST00000309983.4:c.297T>A ENSP00000312304.4:p.Phe99Leu
NM_000367.3:c.297T>A NP_000358.1:p.Phe99Leu
XM_011514839.1:c.297T>A XP_011513141.1:p.Phe99Leu
XM_011514840.1:c.228T>A XP_011513142.1:p.Phe76Leu
NM_000367.4:c.297T>A NP_000358.1:p.Phe99Leu
NM_001346817.1:c.297T>A NP_001333746.1:p.Phe99Leu
NM_001346818.1:c.297T>A NP_001333747.1:p.Phe99Leu
NM_000367.5:c.297T>A MANE Select NP_000358.1:p.Phe99Leu