Canonical Allele Identifier: CA2677457435
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130659_18130660del , CM000668.2:g.18130659_18130660del GRCh38
NC_000006.11:g.18130890_18130891del , CM000668.1:g.18130890_18130891del GRCh37
NC_000006.10:g.18238869_18238870del NCBI36
NG_012137.2:g.29485_29486del
NG_012137.3:g.29485_29486del

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*9_*10del MANE Select ENSP00000312304.4:n.*9_*10del
ENST00000309983.4:c.*9_*10del ENSP00000312304.4:n.*9_*10del
NM_000367.3:c.*9_*10del NP_000358.1:n.*9_*10del
XM_011514839.1:c.*9_*10del XP_011513141.1:n.*9_*10del
XM_011514840.1:c.*9_*10del XP_011513142.1:n.*9_*10del
NM_000367.4:c.*9_*10del NP_000358.1:n.*9_*10del
NM_001346817.1:c.*9_*10del NP_001333746.1:n.*9_*10del
NM_001346818.1:c.*9_*10del NP_001333747.1:n.*9_*10del
NM_000367.5:c.*9_*10del MANE Select NP_000358.1:n.*9_*10del