Canonical Allele Identifier: CA362838405
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18143681A>G , CM000668.2:g.18143681A>G GRCh38
NC_000006.11:g.18143912A>G , CM000668.1:g.18143912A>G GRCh37
NC_000006.10:g.18251891A>G NCBI36
NG_012137.2:g.16463T>C
NG_012137.3:g.16463T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.281T>C MANE Select ENSP00000312304.4:p.Leu94Pro
ENST00000309983.4:c.281T>C ENSP00000312304.4:p.Leu94Pro
NM_000367.3:c.281T>C NP_000358.1:p.Leu94Pro
XM_011514839.1:c.281T>C XP_011513141.1:p.Leu94Pro
XM_011514840.1:c.212T>C XP_011513142.1:p.Leu71Pro
NM_000367.4:c.281T>C NP_000358.1:p.Leu94Pro
NM_001346817.1:c.281T>C NP_001333746.1:p.Leu94Pro
NM_001346818.1:c.281T>C NP_001333747.1:p.Leu94Pro
NM_000367.5:c.281T>C MANE Select NP_000358.1:p.Leu94Pro