Canonical Allele Identifier: CA1613558382

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18139372G= , CM000668.2:g.18139372G=	GRCh38
NC_000006.11:g.18139603G= , CM000668.1:g.18139603G=	GRCh37
NC_000006.10:g.18247582G=	NCBI36
NG_012137.2:g.20772C=
NG_012137.3:g.20772C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.419+293C= MANE Select	ENSP00000312304.4:n.419+293C=
ENST00000309983.4:c.419+293C=	ENSP00000312304.4:n.419+293C=
NM_000367.3:c.419+293C=	NP_000358.1:n.419+293C=
XM_011514839.1:c.419+293C=	XP_011513141.1:n.419+293C=
XM_011514840.1:c.350+293C=	XP_011513142.1:n.350+293C=
NM_000367.4:c.419+293C=	NP_000358.1:n.419+293C=
NM_001346817.1:c.419+293C=	NP_001333746.1:n.419+293C=
NM_001346818.1:c.419+293C=	NP_001333747.1:n.419+293C=
NM_000367.5:c.419+293C= MANE Select	NP_000358.1:n.419+293C=