Canonical Allele Identifier: CA2770170789

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130533_18130534insTGGCTTTTTAGTAAA , CM000668.2:g.18130533_18130534insTGGCTTTTTAGTAAA	GRCh38
NC_000006.11:g.18130764_18130765insTGGCTTTTTAGTAAA , CM000668.1:g.18130764_18130765insTGGCTTTTTAGTAAA	GRCh37
NC_000006.10:g.18238743_18238744insTGGCTTTTTAGTAAA	NCBI36
NG_012137.2:g.29613_29614insACTAAAAAGCCATTT
NG_012137.3:g.29613_29614insACTAAAAAGCCATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.*137_*138insACTAAAAAGCCATTT MANE Select	ENSP00000312304.4:n.*137_*138insACTAAAAAGCCATTT
ENST00000309983.4:c.*137_*138insACTAAAAAGCCATTT	ENSP00000312304.4:n.*137_*138insACTAAAAAGCCATTT
NM_000367.3:c.*137_*138insACTAAAAAGCCATTT	NP_000358.1:n.*137_*138insACTAAAAAGCCATTT
XM_011514839.1:c.*137_*138insACTAAAAAGCCATTT	XP_011513141.1:n.*137_*138insACTAAAAAGCCATTT
XM_011514840.1:c.*137_*138insACTAAAAAGCCATTT	XP_011513142.1:n.*137_*138insACTAAAAAGCCATTT
NM_000367.4:c.*137_*138insACTAAAAAGCCATTT	NP_000358.1:n.*137_*138insACTAAAAAGCCATTT
NM_001346817.1:c.*137_*138insACTAAAAAGCCATTT	NP_001333746.1:n.*137_*138insACTAAAAAGCCATTT
NM_001346818.1:c.*137_*138insACTAAAAAGCCATTT	NP_001333747.1:n.*137_*138insACTAAAAAGCCATTT
NM_000367.5:c.*137_*138insACTAAAAAGCCATTT MANE Select	NP_000358.1:n.*137_*138insACTAAAAAGCCATTT