Canonical Allele Identifier: CA1613545720

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130677T= , CM000668.2:g.18130677T=	GRCh38
NC_000006.11:g.18130908T= , CM000668.1:g.18130908T=	GRCh37
NC_000006.10:g.18238887T=	NCBI36
NG_012137.2:g.29467A=
NG_012137.3:g.29467A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.729A= MANE Select	ENSP00000312304.4:p.Thr243=
ENST00000309983.4:c.729A=	ENSP00000312304.4:p.Thr243=
NM_000367.3:c.729A=	NP_000358.1:p.Thr243=
XM_011514839.1:c.684A=	XP_011513141.1:p.Thr228=
XM_011514840.1:c.660A=	XP_011513142.1:p.Thr220=
NM_000367.4:c.729A=	NP_000358.1:p.Thr243=
NM_001346817.1:c.729A=	NP_001333746.1:p.Thr243=
NM_001346818.1:c.684A=	NP_001333747.1:p.Thr228=
NM_000367.5:c.729A= MANE Select	NP_000358.1:p.Thr243=