Canonical Allele Identifier: CA1613545674
Gene: TPMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130637_18130638delinsTC , CM000668.2:g.18130637_18130638delinsTC GRCh38
NC_000006.11:g.18130868_18130869delinsTC , CM000668.1:g.18130868_18130869delinsTC GRCh37
NC_000006.10:g.18238847_18238848delinsTC NCBI36
NG_012137.2:g.29506_29507delinsGA
NG_012137.3:g.29506_29507delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.*30_*31delinsGA MANE Select ENSP00000312304.4:n.*30_*31delinsGA
ENST00000309983.4:c.*30_*31delinsGA ENSP00000312304.4:n.*30_*31delinsGA
NM_000367.3:c.*30_*31delinsGA NP_000358.1:n.*30_*31delinsGA
XM_011514839.1:c.*30_*31delinsGA XP_011513141.1:n.*30_*31delinsGA
XM_011514840.1:c.*30_*31delinsGA XP_011513142.1:n.*30_*31delinsGA
NM_000367.4:c.*30_*31delinsGA NP_000358.1:n.*30_*31delinsGA
NM_001346817.1:c.*30_*31delinsGA NP_001333746.1:n.*30_*31delinsGA
NM_001346818.1:c.*30_*31delinsGA NP_001333747.1:n.*30_*31delinsGA
NM_000367.5:c.*30_*31delinsGA MANE Select NP_000358.1:n.*30_*31delinsGA