Canonical Allele Identifier: CA1613557367

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18138825_18138841delinsGATTTAGGTTTTTATAA , CM000668.2:g.18138825_18138841delinsGATTTAGGTTTTTATAA	GRCh38
NC_000006.11:g.18139056_18139072delinsGATTTAGGTTTTTATAA , CM000668.1:g.18139056_18139072delinsGATTTAGGTTTTTATAA	GRCh37
NC_000006.10:g.18247035_18247051delinsGATTTAGGTTTTTATAA	NCBI36
NG_012137.2:g.21303_21319delinsTTATAAAAACCTAAATC
NG_012137.3:g.21303_21319delinsTTATAAAAACCTAAATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.494+122_494+138delinsTTATAAAAACCTAAATC MANE Select	ENSP00000312304.4:n.494+122_494+138delinsTTATAAAAACCTAAATC
ENST00000309983.4:c.494+122_494+138delinsTTATAAAAACCTAAATC	ENSP00000312304.4:n.494+122_494+138delinsTTATAAAAACCTAAATC
NM_000367.3:c.494+122_494+138delinsTTATAAAAACCTAAATC	NP_000358.1:n.494+122_494+138delinsTTATAAAAACCTAAATC
XM_011514839.1:c.494+122_494+138delinsTTATAAAAACCTAAATC	XP_011513141.1:n.494+122_494+138delinsTTATAAAAACCTAAATC
XM_011514840.1:c.425+122_425+138delinsTTATAAAAACCTAAATC	XP_011513142.1:n.425+122_425+138delinsTTATAAAAACCTAAATC
NM_000367.4:c.494+122_494+138delinsTTATAAAAACCTAAATC	NP_000358.1:n.494+122_494+138delinsTTATAAAAACCTAAATC
NM_001346817.1:c.494+122_494+138delinsTTATAAAAACCTAAATC	NP_001333746.1:n.494+122_494+138delinsTTATAAAAACCTAAATC
NM_001346818.1:c.494+122_494+138delinsTTATAAAAACCTAAATC	NP_001333747.1:n.494+122_494+138delinsTTATAAAAACCTAAATC
NM_000367.5:c.494+122_494+138delinsTTATAAAAACCTAAATC MANE Select	NP_000358.1:n.494+122_494+138delinsTTATAAAAACCTAAATC