Canonical Allele Identifier: CA134961564

Gene: TPMT

Linked Data

• dbSNP Id: rs377085266
• MyVariant Identifiers: chr6:g.18131003A>G (hg19) ; chr6:g.18130772A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130772A>G , CM000668.2:g.18130772A>G	GRCh38
NC_000006.11:g.18131003A>G , CM000668.1:g.18131003A>G	GRCh37
NC_000006.10:g.18238982A>G	NCBI36
NG_012137.2:g.29372T>C
NG_012137.3:g.29372T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.634T>C MANE Select	ENSP00000312304.4:p.Cys212Arg
ENST00000309983.4:c.634T>C	ENSP00000312304.4:p.Cys212Arg
NM_000367.3:c.634T>C	NP_000358.1:p.Cys212Arg
XM_011514839.1:c.589T>C	XP_011513141.1:p.Cys197Arg
XM_011514840.1:c.565T>C	XP_011513142.1:p.Cys189Arg
NM_000367.4:c.634T>C	NP_000358.1:p.Cys212Arg
NM_001346817.1:c.634T>C	NP_001333746.1:p.Cys212Arg
NM_001346818.1:c.589T>C	NP_001333747.1:p.Cys197Arg
NM_000367.5:c.634T>C MANE Select	NP_000358.1:p.Cys212Arg