Canonical Allele Identifier: CA1613545554

Gene: TPMT

Linked Data

• dbSNP Id: rs1783921223

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130530A>C , CM000668.2:g.18130530A>C	GRCh38
NC_000006.11:g.18130761A>C , CM000668.1:g.18130761A>C	GRCh37
NC_000006.10:g.18238740A>C	NCBI36
NG_012137.2:g.29614T>G
NG_012137.3:g.29614T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.*138T>G MANE Select	ENSP00000312304.4:n.*138T>G
ENST00000309983.4:c.*138T>G	ENSP00000312304.4:n.*138T>G
NM_000367.3:c.*138T>G	NP_000358.1:n.*138T>G
XM_011514839.1:c.*138T>G	XP_011513141.1:n.*138T>G
XM_011514840.1:c.*138T>G	XP_011513142.1:n.*138T>G
NM_000367.4:c.*138T>G	NP_000358.1:n.*138T>G
NM_001346817.1:c.*138T>G	NP_001333746.1:n.*138T>G
NM_001346818.1:c.*138T>G	NP_001333747.1:n.*138T>G
NM_000367.5:c.*138T>G MANE Select	NP_000358.1:n.*138T>G