Canonical Allele Identifier: CA1613558189
Gene: TPMT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18139274G= , CM000668.2:g.18139274G= GRCh38
NC_000006.11:g.18139505G= , CM000668.1:g.18139505G= GRCh37
NC_000006.10:g.18247484G= NCBI36
NG_012137.2:g.20870C=
NG_012137.3:g.20870C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.420-237C= MANE Select ENSP00000312304.4:n.420-237C=
ENST00000309983.4:c.420-237C= ENSP00000312304.4:n.420-237C=
NM_000367.3:c.420-237C= NP_000358.1:n.420-237C=
XM_011514839.1:c.420-237C= XP_011513141.1:n.420-237C=
XM_011514840.1:c.351-237C= XP_011513142.1:n.351-237C=
NM_000367.4:c.420-237C= NP_000358.1:n.420-237C=
NM_001346817.1:c.420-237C= NP_001333746.1:n.420-237C=
NM_001346818.1:c.420-237C= NP_001333747.1:n.420-237C=
NM_000367.5:c.420-237C= MANE Select NP_000358.1:n.420-237C=
Search 100 bp 5'
Search 100 bp 3'