Canonical Allele Identifier: CA2677458265
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18143762del , CM000668.2:g.18143762del GRCh38
NC_000006.11:g.18143993del , CM000668.1:g.18143993del GRCh37
NC_000006.10:g.18251972del NCBI36
NG_012137.2:g.16382del
NG_012137.3:g.16382del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.234-34del MANE Select ENSP00000312304.4:n.234-34del
ENST00000309983.4:c.234-34del ENSP00000312304.4:n.234-34del
NM_000367.3:c.234-34del NP_000358.1:n.234-34del
XM_011514839.1:c.234-34del XP_011513141.1:n.234-34del
XM_011514840.1:c.165-34del XP_011513142.1:n.165-34del
NM_000367.4:c.234-34del NP_000358.1:n.234-34del
NM_001346817.1:c.234-34del NP_001333746.1:n.234-34del
NM_001346818.1:c.234-34del NP_001333747.1:n.234-34del
NM_000367.5:c.234-34del MANE Select NP_000358.1:n.234-34del