Canonical Allele Identifier: CA1613545547

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130525T= , CM000668.2:g.18130525T=	GRCh38
NC_000006.11:g.18130756T= , CM000668.1:g.18130756T=	GRCh37
NC_000006.10:g.18238735T=	NCBI36
NG_012137.2:g.29619A=
NG_012137.3:g.29619A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.*143A= MANE Select	ENSP00000312304.4:n.*143A=
ENST00000309983.4:c.*143A=	ENSP00000312304.4:n.*143A=
NM_000367.3:c.*143A=	NP_000358.1:n.*143A=
XM_011514839.1:c.*143A=	XP_011513141.1:n.*143A=
XM_011514840.1:c.*143A=	XP_011513142.1:n.*143A=
NM_000367.4:c.*143A=	NP_000358.1:n.*143A=
NM_001346817.1:c.*143A=	NP_001333746.1:n.*143A=
NM_001346818.1:c.*143A=	NP_001333747.1:n.*143A=
NM_000367.5:c.*143A= MANE Select	NP_000358.1:n.*143A=