Canonical Allele Identifier: CA134961531
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs1007532303
gnomAD v3: 6-18130535-C-A
gnomAD v4: 6-18130535-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130535C>A , CM000668.2:g.18130535C>A GRCh38
NC_000006.11:g.18130766C>A , CM000668.1:g.18130766C>A GRCh37
NC_000006.10:g.18238745C>A NCBI36
NG_012137.2:g.29609G>T
NG_012137.3:g.29609G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*133G>T MANE Select ENSP00000312304.4:n.*133G>T
ENST00000309983.4:c.*133G>T ENSP00000312304.4:n.*133G>T
NM_000367.3:c.*133G>T NP_000358.1:n.*133G>T
XM_011514839.1:c.*133G>T XP_011513141.1:n.*133G>T
XM_011514840.1:c.*133G>T XP_011513142.1:n.*133G>T
NM_000367.4:c.*133G>T NP_000358.1:n.*133G>T
NM_001346817.1:c.*133G>T NP_001333746.1:n.*133G>T
NM_001346818.1:c.*133G>T NP_001333747.1:n.*133G>T
NM_000367.5:c.*133G>T MANE Select NP_000358.1:n.*133G>T