Canonical Allele Identifier: CA362832194
Gene: TPMT HGNC NCBI

Linked Data

gnomAD v4: 6-18130703-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130703G>T , CM000668.2:g.18130703G>T GRCh38
NC_000006.11:g.18130934G>T , CM000668.1:g.18130934G>T GRCh37
NC_000006.10:g.18238913G>T NCBI36
NG_012137.2:g.29441C>A
NG_012137.3:g.29441C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.703C>A MANE Select ENSP00000312304.4:p.Leu235Ile
ENST00000309983.4:c.703C>A ENSP00000312304.4:p.Leu235Ile
NM_000367.3:c.703C>A NP_000358.1:p.Leu235Ile
XM_011514839.1:c.658C>A XP_011513141.1:p.Leu220Ile
XM_011514840.1:c.634C>A XP_011513142.1:p.Leu212Ile
NM_000367.4:c.703C>A NP_000358.1:p.Leu235Ile
NM_001346817.1:c.703C>A NP_001333746.1:p.Leu235Ile
NM_001346818.1:c.658C>A NP_001333747.1:p.Leu220Ile
NM_000367.5:c.703C>A MANE Select NP_000358.1:p.Leu235Ile