Canonical Allele Identifier: CA448764671
Gene: TPMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.18130932A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130701A>C , CM000668.2:g.18130701A>C GRCh38
NC_000006.11:g.18130932A>C , CM000668.1:g.18130932A>C GRCh37
NC_000006.10:g.18238911A>C NCBI36
NG_012137.2:g.29443T>G
NG_012137.3:g.29443T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.705T>G MANE Select ENSP00000312304.4:p.Leu235=
ENST00000309983.4:c.705T>G ENSP00000312304.4:p.Leu235=
NM_000367.3:c.705T>G NP_000358.1:p.Leu235=
XM_011514839.1:c.660T>G XP_011513141.1:p.Leu220=
XM_011514840.1:c.636T>G XP_011513142.1:p.Leu212=
NM_000367.4:c.705T>G NP_000358.1:p.Leu235=
NM_001346817.1:c.705T>G NP_001333746.1:p.Leu235=
NM_001346818.1:c.660T>G NP_001333747.1:p.Leu220=
NM_000367.5:c.705T>G MANE Select NP_000358.1:p.Leu235=