Canonical Allele Identifier: CA1613558625

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18139533C= , CM000668.2:g.18139533C=	GRCh38
NC_000006.11:g.18139764C= , CM000668.1:g.18139764C=	GRCh37
NC_000006.10:g.18247743C=	NCBI36
NG_012137.2:g.20611G=
NG_012137.3:g.20611G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.419+132G= MANE Select	ENSP00000312304.4:n.419+132G=
ENST00000309983.4:c.419+132G=	ENSP00000312304.4:n.419+132G=
NM_000367.3:c.419+132G=	NP_000358.1:n.419+132G=
XM_011514839.1:c.419+132G=	XP_011513141.1:n.419+132G=
XM_011514840.1:c.350+132G=	XP_011513142.1:n.350+132G=
NM_000367.4:c.419+132G=	NP_000358.1:n.419+132G=
NM_001346817.1:c.419+132G=	NP_001333746.1:n.419+132G=
NM_001346818.1:c.419+132G=	NP_001333747.1:n.419+132G=
NM_000367.5:c.419+132G= MANE Select	NP_000358.1:n.419+132G=