Canonical Allele Identifier: CA448765722

Gene: TPMT

Linked Data

• MyVariant Identifiers: chr6:g.18143866T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18143635T>C , CM000668.2:g.18143635T>C	GRCh38
NC_000006.11:g.18143866T>C , CM000668.1:g.18143866T>C	GRCh37
NC_000006.10:g.18251845T>C	NCBI36
NG_012137.2:g.16509A>G
NG_012137.3:g.16509A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.327A>G MANE Select	ENSP00000312304.4:p.Glu109=
ENST00000309983.4:c.327A>G	ENSP00000312304.4:p.Glu109=
NM_000367.3:c.327A>G	NP_000358.1:p.Glu109=
XM_011514839.1:c.327A>G	XP_011513141.1:p.Glu109=
XM_011514840.1:c.258A>G	XP_011513142.1:p.Glu86=
NM_000367.4:c.327A>G	NP_000358.1:p.Glu109=
NM_001346817.1:c.327A>G	NP_001333746.1:p.Glu109=
NM_001346818.1:c.327A>G	NP_001333747.1:p.Glu109=
NM_000367.5:c.327A>G MANE Select	NP_000358.1:p.Glu109=