Canonical Allele Identifier: CA1613558594

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18139509T= , CM000668.2:g.18139509T=	GRCh38
NC_000006.11:g.18139740T= , CM000668.1:g.18139740T=	GRCh37
NC_000006.10:g.18247719T=	NCBI36
NG_012137.2:g.20635A=
NG_012137.3:g.20635A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.419+156A= MANE Select	ENSP00000312304.4:n.419+156A=
ENST00000309983.4:c.419+156A=	ENSP00000312304.4:n.419+156A=
NM_000367.3:c.419+156A=	NP_000358.1:n.419+156A=
XM_011514839.1:c.419+156A=	XP_011513141.1:n.419+156A=
XM_011514840.1:c.350+156A=	XP_011513142.1:n.350+156A=
NM_000367.4:c.419+156A=	NP_000358.1:n.419+156A=
NM_001346817.1:c.419+156A=	NP_001333746.1:n.419+156A=
NM_001346818.1:c.419+156A=	NP_001333747.1:n.419+156A=
NM_000367.5:c.419+156A= MANE Select	NP_000358.1:n.419+156A=