Canonical Allele Identifier: CA362835628

Gene: TPMT

Linked Data

• MyVariant Identifiers: chr6:g.18139244C>T (hg19) ; chr6:g.18139013C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18139013C>T , CM000668.2:g.18139013C>T	GRCh38
NC_000006.11:g.18139244C>T , CM000668.1:g.18139244C>T	GRCh37
NC_000006.10:g.18247223C>T	NCBI36
NG_012137.2:g.21131G>A
NG_012137.3:g.21131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.444G>A MANE Select	ENSP00000312304.4:p.Met148Ile
ENST00000309983.4:c.444G>A	ENSP00000312304.4:p.Met148Ile
NM_000367.3:c.444G>A	NP_000358.1:p.Met148Ile
XM_011514839.1:c.444G>A	XP_011513141.1:p.Met148Ile
XM_011514840.1:c.375G>A	XP_011513142.1:p.Met125Ile
NM_000367.4:c.444G>A	NP_000358.1:p.Met148Ile
NM_001346817.1:c.444G>A	NP_001333746.1:p.Met148Ile
NM_001346818.1:c.444G>A	NP_001333747.1:p.Met148Ile
NM_000367.5:c.444G>A MANE Select	NP_000358.1:p.Met148Ile