Canonical Allele Identifier: CA1613545753
Gene: TPMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130705C= , CM000668.2:g.18130705C= GRCh38
NC_000006.11:g.18130936C= , CM000668.1:g.18130936C= GRCh37
NC_000006.10:g.18238915C= NCBI36
NG_012137.2:g.29439G=
NG_012137.3:g.29439G=

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.701G= MANE Select ENSP00000312304.4:p.Cys234=
ENST00000309983.4:c.701G= ENSP00000312304.4:p.Cys234=
NM_000367.3:c.701G= NP_000358.1:p.Cys234=
XM_011514839.1:c.656G= XP_011513141.1:p.Cys219=
XM_011514840.1:c.632G= XP_011513142.1:p.Cys211=
NM_000367.4:c.701G= NP_000358.1:p.Cys234=
NM_001346817.1:c.701G= NP_001333746.1:p.Cys234=
NM_001346818.1:c.656G= NP_001333747.1:p.Cys219=
NM_000367.5:c.701G= MANE Select NP_000358.1:p.Cys234=