Canonical Allele Identifier: CA2770171182
Gene: TPMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18139605G>A , CM000668.2:g.18139605G>A GRCh38
NC_000006.11:g.18139836G>A , CM000668.1:g.18139836G>A GRCh37
NC_000006.10:g.18247815G>A NCBI36
NG_012137.2:g.20539C>T
NG_012137.3:g.20539C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.419+60C>T MANE Select ENSP00000312304.4:n.419+60C>T
ENST00000309983.4:c.419+60C>T ENSP00000312304.4:n.419+60C>T
NM_000367.3:c.419+60C>T NP_000358.1:n.419+60C>T
XM_011514839.1:c.419+60C>T XP_011513141.1:n.419+60C>T
XM_011514840.1:c.350+60C>T XP_011513142.1:n.350+60C>T
NM_000367.4:c.419+60C>T NP_000358.1:n.419+60C>T
NM_001346817.1:c.419+60C>T NP_001333746.1:n.419+60C>T
NM_001346818.1:c.419+60C>T NP_001333747.1:n.419+60C>T
NM_000367.5:c.419+60C>T MANE Select NP_000358.1:n.419+60C>T
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