Canonical Allele Identifier: CA1613558258
Gene: TPMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18139294G= , CM000668.2:g.18139294G= GRCh38
NC_000006.11:g.18139525G= , CM000668.1:g.18139525G= GRCh37
NC_000006.10:g.18247504G= NCBI36
NG_012137.2:g.20850C=
NG_012137.3:g.20850C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.420-257C= MANE Select ENSP00000312304.4:n.420-257C=
ENST00000309983.4:c.420-257C= ENSP00000312304.4:n.420-257C=
NM_000367.3:c.420-257C= NP_000358.1:n.420-257C=
XM_011514839.1:c.420-257C= XP_011513141.1:n.420-257C=
XM_011514840.1:c.351-257C= XP_011513142.1:n.351-257C=
NM_000367.4:c.420-257C= NP_000358.1:n.420-257C=
NM_001346817.1:c.420-257C= NP_001333746.1:n.420-257C=
NM_001346818.1:c.420-257C= NP_001333747.1:n.420-257C=
NM_000367.5:c.420-257C= MANE Select NP_000358.1:n.420-257C=
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