Canonical Allele Identifier: CA650822497

Gene: TPMT

Linked Data

• COSMIC: COSN20783461

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130448_18130449insT , CM000668.2:g.18130448_18130449insT	GRCh38
NC_000006.11:g.18130679_18130680insT , CM000668.1:g.18130679_18130680insT	GRCh37
NC_000006.10:g.18238658_18238659insT	NCBI36
NG_012137.2:g.29695_29696insA
NG_012137.3:g.29695_29696insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.*219_*220insA MANE Select	ENSP00000312304.4:n.*219_*220insA
ENST00000309983.4:c.*219_*220insA	ENSP00000312304.4:n.*219_*220insA
NM_000367.3:c.*219_*220insA	NP_000358.1:n.*219_*220insA
XM_011514839.1:c.*219_*220insA	XP_011513141.1:n.*219_*220insA
XM_011514840.1:c.*219_*220insA	XP_011513142.1:n.*219_*220insA
NM_000367.4:c.*219_*220insA	NP_000358.1:n.*219_*220insA
NM_001346817.1:c.*219_*220insA	NP_001333746.1:n.*219_*220insA
NM_001346818.1:c.*219_*220insA	NP_001333747.1:n.*219_*220insA
NM_000367.5:c.*219_*220insA MANE Select	NP_000358.1:n.*219_*220insA