Canonical Allele Identifier: CA448764667
Gene: TPMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.18130923C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130692C>T , CM000668.2:g.18130692C>T GRCh38
NC_000006.11:g.18130923C>T , CM000668.1:g.18130923C>T GRCh37
NC_000006.10:g.18238902C>T NCBI36
NG_012137.2:g.29452G>A
NG_012137.3:g.29452G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.714G>A MANE Select ENSP00000312304.4:p.Lys238=
ENST00000309983.4:c.714G>A ENSP00000312304.4:p.Lys238=
NM_000367.3:c.714G>A NP_000358.1:p.Lys238=
XM_011514839.1:c.669G>A XP_011513141.1:p.Lys223=
XM_011514840.1:c.645G>A XP_011513142.1:p.Lys215=
NM_000367.4:c.714G>A NP_000358.1:p.Lys238=
NM_001346817.1:c.714G>A NP_001333746.1:p.Lys238=
NM_001346818.1:c.669G>A NP_001333747.1:p.Lys223=
NM_000367.5:c.714G>A MANE Select NP_000358.1:p.Lys238=