Canonical Allele Identifier: CA1613557498
Gene: TPMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18138933C= , CM000668.2:g.18138933C= GRCh38
NC_000006.11:g.18139164C= , CM000668.1:g.18139164C= GRCh37
NC_000006.10:g.18247143C= NCBI36
NG_012137.2:g.21211G=
NG_012137.3:g.21211G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.494+30G= MANE Select ENSP00000312304.4:n.494+30G=
ENST00000309983.4:c.494+30G= ENSP00000312304.4:n.494+30G=
NM_000367.3:c.494+30G= NP_000358.1:n.494+30G=
XM_011514839.1:c.494+30G= XP_011513141.1:n.494+30G=
XM_011514840.1:c.425+30G= XP_011513142.1:n.425+30G=
NM_000367.4:c.494+30G= NP_000358.1:n.494+30G=
NM_001346817.1:c.494+30G= NP_001333746.1:n.494+30G=
NM_001346818.1:c.494+30G= NP_001333747.1:n.494+30G=
NM_000367.5:c.494+30G= MANE Select NP_000358.1:n.494+30G=