Canonical Allele Identifier: CA1613545741
Gene: TPMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130688A= , CM000668.2:g.18130688A= GRCh38
NC_000006.11:g.18130919A= , CM000668.1:g.18130919A= GRCh37
NC_000006.10:g.18238898A= NCBI36
NG_012137.2:g.29456T=
NG_012137.3:g.29456T=

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.718T= MANE Select ENSP00000312304.4:p.Tyr240=
ENST00000309983.4:c.718T= ENSP00000312304.4:p.Tyr240=
NM_000367.3:c.718T= NP_000358.1:p.Tyr240=
XM_011514839.1:c.673T= XP_011513141.1:p.Tyr225=
XM_011514840.1:c.649T= XP_011513142.1:p.Tyr217=
NM_000367.4:c.718T= NP_000358.1:p.Tyr240=
NM_001346817.1:c.718T= NP_001333746.1:p.Tyr240=
NM_001346818.1:c.673T= NP_001333747.1:p.Tyr225=
NM_000367.5:c.718T= MANE Select NP_000358.1:p.Tyr240=