Canonical Allele Identifier: CA1613545684

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130644_18130649delinsGATTTT , CM000668.2:g.18130644_18130649delinsGATTTT	GRCh38
NC_000006.11:g.18130875_18130880delinsGATTTT , CM000668.1:g.18130875_18130880delinsGATTTT	GRCh37
NC_000006.10:g.18238854_18238859delinsGATTTT	NCBI36
NG_012137.2:g.29495_29500delinsAAAATC
NG_012137.3:g.29495_29500delinsAAAATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.*19_*24delinsAAAATC MANE Select	ENSP00000312304.4:n.*19_*24delinsAAAATC
ENST00000309983.4:c.*19_*24delinsAAAATC	ENSP00000312304.4:n.*19_*24delinsAAAATC
NM_000367.3:c.*19_*24delinsAAAATC	NP_000358.1:n.*19_*24delinsAAAATC
XM_011514839.1:c.*19_*24delinsAAAATC	XP_011513141.1:n.*19_*24delinsAAAATC
XM_011514840.1:c.*19_*24delinsAAAATC	XP_011513142.1:n.*19_*24delinsAAAATC
NM_000367.4:c.*19_*24delinsAAAATC	NP_000358.1:n.*19_*24delinsAAAATC
NM_001346817.1:c.*19_*24delinsAAAATC	NP_001333746.1:n.*19_*24delinsAAAATC
NM_001346818.1:c.*19_*24delinsAAAATC	NP_001333747.1:n.*19_*24delinsAAAATC
NM_000367.5:c.*19_*24delinsAAAATC MANE Select	NP_000358.1:n.*19_*24delinsAAAATC