Canonical Allele Identifier: CA1613545764

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130712T= , CM000668.2:g.18130712T=	GRCh38
NC_000006.11:g.18130943T= , CM000668.1:g.18130943T=	GRCh37
NC_000006.10:g.18238922T=	NCBI36
NG_012137.2:g.29432A=
NG_012137.3:g.29432A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.694A= MANE Select	ENSP00000312304.4:p.Ile232=
ENST00000309983.4:c.694A=	ENSP00000312304.4:p.Ile232=
NM_000367.3:c.694A=	NP_000358.1:p.Ile232=
XM_011514839.1:c.649A=	XP_011513141.1:p.Ile217=
XM_011514840.1:c.625A=	XP_011513142.1:p.Ile209=
NM_000367.4:c.694A=	NP_000358.1:p.Ile232=
NM_001346817.1:c.694A=	NP_001333746.1:p.Ile232=
NM_001346818.1:c.649A=	NP_001333747.1:p.Ile217=
NM_000367.5:c.694A= MANE Select	NP_000358.1:p.Ile232=