Canonical Allele Identifier: CA1613545798

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130736_18130737delinsCA , CM000668.2:g.18130736_18130737delinsCA	GRCh38
NC_000006.11:g.18130967_18130968delinsCA , CM000668.1:g.18130967_18130968delinsCA	GRCh37
NC_000006.10:g.18238946_18238947delinsCA	NCBI36
NG_012137.2:g.29407_29408delinsTG
NG_012137.3:g.29407_29408delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.669_670delinsTG MANE Select	ENSP00000312304.4:p.Phe223=
ENST00000309983.4:c.669_670delinsTG	ENSP00000312304.4:p.Phe223=
NM_000367.3:c.669_670delinsTG	NP_000358.1:p.Phe223=
XM_011514839.1:c.624_625delinsTG	XP_011513141.1:p.Phe208=
XM_011514840.1:c.600_601delinsTG	XP_011513142.1:p.Phe200=
NM_000367.4:c.669_670delinsTG	NP_000358.1:p.Phe223=
NM_001346817.1:c.669_670delinsTG	NP_001333746.1:p.Phe223=
NM_001346818.1:c.624_625delinsTG	NP_001333747.1:p.Phe208=
NM_000367.5:c.669_670delinsTG MANE Select	NP_000358.1:p.Phe223=