Canonical Allele Identifier: CA362838308

Gene: TPMT

Linked Data

• MyVariant Identifiers: chr6:g.18143886G>C (hg19) ; chr6:g.18143655G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18143655G>C , CM000668.2:g.18143655G>C	GRCh38
NC_000006.11:g.18143886G>C , CM000668.1:g.18143886G>C	GRCh37
NC_000006.10:g.18251865G>C	NCBI36
NG_012137.2:g.16489C>G
NG_012137.3:g.16489C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.307C>G MANE Select	ENSP00000312304.4:p.Gln103Glu
ENST00000309983.4:c.307C>G	ENSP00000312304.4:p.Gln103Glu
NM_000367.3:c.307C>G	NP_000358.1:p.Gln103Glu
XM_011514839.1:c.307C>G	XP_011513141.1:p.Gln103Glu
XM_011514840.1:c.238C>G	XP_011513142.1:p.Gln80Glu
NM_000367.4:c.307C>G	NP_000358.1:p.Gln103Glu
NM_001346817.1:c.307C>G	NP_001333746.1:p.Gln103Glu
NM_001346818.1:c.307C>G	NP_001333747.1:p.Gln103Glu
NM_000367.5:c.307C>G MANE Select	NP_000358.1:p.Gln103Glu