Canonical Allele Identifier: CA362838242
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs1248105963
gnomAD v2: 6-18143868-C-T
gnomAD v4: 6-18143637-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18143637C>T , CM000668.2:g.18143637C>T GRCh38
NC_000006.11:g.18143868C>T , CM000668.1:g.18143868C>T GRCh37
NC_000006.10:g.18251847C>T NCBI36
NG_012137.2:g.16507G>A
NG_012137.3:g.16507G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.325G>A MANE Select ENSP00000312304.4:p.Glu109Lys
ENST00000309983.4:c.325G>A ENSP00000312304.4:p.Glu109Lys
NM_000367.3:c.325G>A NP_000358.1:p.Glu109Lys
XM_011514839.1:c.325G>A XP_011513141.1:p.Glu109Lys
XM_011514840.1:c.256G>A XP_011513142.1:p.Glu86Lys
NM_000367.4:c.325G>A NP_000358.1:p.Glu109Lys
NM_001346817.1:c.325G>A NP_001333746.1:p.Glu109Lys
NM_001346818.1:c.325G>A NP_001333747.1:p.Glu109Lys
NM_000367.5:c.325G>A MANE Select NP_000358.1:p.Glu109Lys