Canonical Allele Identifier: CA1613545969

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130887C= , CM000668.2:g.18130887C=	GRCh38
NC_000006.11:g.18131118C= , CM000668.1:g.18131118C=	GRCh37
NC_000006.10:g.18239097C=	NCBI36
NG_012137.2:g.29257G=
NG_012137.3:g.29257G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.626-107G= MANE Select	ENSP00000312304.4:n.626-107G=
ENST00000309983.4:c.626-107G=	ENSP00000312304.4:n.626-107G=
NM_000367.3:c.626-107G=	NP_000358.1:n.626-107G=
XM_011514839.1:c.581-107G=	XP_011513141.1:n.581-107G=
XM_011514840.1:c.557-107G=	XP_011513142.1:n.557-107G=
NM_000367.4:c.626-107G=	NP_000358.1:n.626-107G=
NM_001346817.1:c.626-107G=	NP_001333746.1:n.626-107G=
NM_001346818.1:c.581-107G=	NP_001333747.1:n.581-107G=
NM_000367.5:c.626-107G= MANE Select	NP_000358.1:n.626-107G=