Canonical Allele Identifier: CA1613545664
Gene: TPMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130627C= , CM000668.2:g.18130627C= GRCh38
NC_000006.11:g.18130858C= , CM000668.1:g.18130858C= GRCh37
NC_000006.10:g.18238837C= NCBI36
NG_012137.2:g.29517G=
NG_012137.3:g.29517G=

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*41G= MANE Select ENSP00000312304.4:n.*41G=
ENST00000309983.4:c.*41G= ENSP00000312304.4:n.*41G=
NM_000367.3:c.*41G= NP_000358.1:n.*41G=
XM_011514839.1:c.*41G= XP_011513141.1:n.*41G=
XM_011514840.1:c.*41G= XP_011513142.1:n.*41G=
NM_000367.4:c.*41G= NP_000358.1:n.*41G=
NM_001346817.1:c.*41G= NP_001333746.1:n.*41G=
NM_001346818.1:c.*41G= NP_001333747.1:n.*41G=
NM_000367.5:c.*41G= MANE Select NP_000358.1:n.*41G=