Canonical Allele Identifier: CA1613557362

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18138819G= , CM000668.2:g.18138819G=	GRCh38
NC_000006.11:g.18139050G= , CM000668.1:g.18139050G=	GRCh37
NC_000006.10:g.18247029G=	NCBI36
NG_012137.2:g.21325C=
NG_012137.3:g.21325C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.494+144C= MANE Select	ENSP00000312304.4:n.494+144C=
ENST00000309983.4:c.494+144C=	ENSP00000312304.4:n.494+144C=
NM_000367.3:c.494+144C=	NP_000358.1:n.494+144C=
XM_011514839.1:c.494+144C=	XP_011513141.1:n.494+144C=
XM_011514840.1:c.425+144C=	XP_011513142.1:n.425+144C=
NM_000367.4:c.494+144C=	NP_000358.1:n.494+144C=
NM_001346817.1:c.494+144C=	NP_001333746.1:n.494+144C=
NM_001346818.1:c.494+144C=	NP_001333747.1:n.494+144C=
NM_000367.5:c.494+144C= MANE Select	NP_000358.1:n.494+144C=