Canonical Allele Identifier: CA448764756

Gene: TPMT

Linked Data

• MyVariant Identifiers: chr6:g.18131001G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130770G>A , CM000668.2:g.18130770G>A	GRCh38
NC_000006.11:g.18131001G>A , CM000668.1:g.18131001G>A	GRCh37
NC_000006.10:g.18238980G>A	NCBI36
NG_012137.2:g.29374C>T
NG_012137.3:g.29374C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.636C>T MANE Select	ENSP00000312304.4:p.Cys212=
ENST00000309983.4:c.636C>T	ENSP00000312304.4:p.Cys212=
NM_000367.3:c.636C>T	NP_000358.1:p.Cys212=
XM_011514839.1:c.591C>T	XP_011513141.1:p.Cys197=
XM_011514840.1:c.567C>T	XP_011513142.1:p.Cys189=
NM_000367.4:c.636C>T	NP_000358.1:p.Cys212=
NM_001346817.1:c.636C>T	NP_001333746.1:p.Cys212=
NM_001346818.1:c.591C>T	NP_001333747.1:p.Cys197=
NM_000367.5:c.636C>T MANE Select	NP_000358.1:p.Cys212=