Canonical Allele Identifier: CA2677458292

Gene: TPMT

Linked Data

• gnomAD v4: 6-18143807-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18143807T>C , CM000668.2:g.18143807T>C	GRCh38
NC_000006.11:g.18144038T>C , CM000668.1:g.18144038T>C	GRCh37
NC_000006.10:g.18252017T>C	NCBI36
NG_012137.2:g.16337A>G
NG_012137.3:g.16337A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.234-79A>G MANE Select	ENSP00000312304.4:n.234-79A>G
ENST00000309983.4:c.234-79A>G	ENSP00000312304.4:n.234-79A>G
NM_000367.3:c.234-79A>G	NP_000358.1:n.234-79A>G
XM_011514839.1:c.234-79A>G	XP_011513141.1:n.234-79A>G
XM_011514840.1:c.165-79A>G	XP_011513142.1:n.165-79A>G
NM_000367.4:c.234-79A>G	NP_000358.1:n.234-79A>G
NM_001346817.1:c.234-79A>G	NP_001333746.1:n.234-79A>G
NM_001346818.1:c.234-79A>G	NP_001333747.1:n.234-79A>G
NM_000367.5:c.234-79A>G MANE Select	NP_000358.1:n.234-79A>G