Canonical Allele Identifier: CA1613565559

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18143723G= , CM000668.2:g.18143723G=	GRCh38
NC_000006.11:g.18143954G= , CM000668.1:g.18143954G=	GRCh37
NC_000006.10:g.18251933G=	NCBI36
NG_012137.2:g.16421C=
NG_012137.3:g.16421C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.239C= MANE Select	ENSP00000312304.4:p.Ala80=
ENST00000309983.4:c.239C=	ENSP00000312304.4:p.Ala80=
NM_000367.3:c.239C=	NP_000358.1:p.Ala80=
XM_011514839.1:c.239C=	XP_011513141.1:p.Ala80=
XM_011514840.1:c.170C=	XP_011513142.1:p.Ala57=
NM_000367.4:c.239C=	NP_000358.1:p.Ala80=
NM_001346817.1:c.239C=	NP_001333746.1:p.Ala80=
NM_001346818.1:c.239C=	NP_001333747.1:p.Ala80=
NM_000367.5:c.239C= MANE Select	NP_000358.1:p.Ala80=