Canonical Allele Identifier: CA2677457499
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130788_18130789insTGTAA , CM000668.2:g.18130788_18130789insTGTAA GRCh38
NC_000006.11:g.18131019_18131020insTGTAA , CM000668.1:g.18131019_18131020insTGTAA GRCh37
NC_000006.10:g.18238998_18238999insTGTAA NCBI36
NG_012137.2:g.29356_29357insTACAT
NG_012137.3:g.29356_29357insTACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.626-8_626-7insTACAT MANE Select ENSP00000312304.4:n.626-8_626-7insTACAT
ENST00000309983.4:c.626-8_626-7insTACAT ENSP00000312304.4:n.626-8_626-7insTACAT
NM_000367.3:c.626-8_626-7insTACAT NP_000358.1:n.626-8_626-7insTACAT
XM_011514839.1:c.581-8_581-7insTACAT XP_011513141.1:n.581-8_581-7insTACAT
XM_011514840.1:c.557-8_557-7insTACAT XP_011513142.1:n.557-8_557-7insTACAT
NM_000367.4:c.626-8_626-7insTACAT NP_000358.1:n.626-8_626-7insTACAT
NM_001346817.1:c.626-8_626-7insTACAT NP_001333746.1:n.626-8_626-7insTACAT
NM_001346818.1:c.581-8_581-7insTACAT NP_001333747.1:n.581-8_581-7insTACAT
NM_000367.5:c.626-8_626-7insTACAT MANE Select NP_000358.1:n.626-8_626-7insTACAT