Canonical Allele Identifier: CA1613545509

Gene: TPMT

Linked Data

• dbSNP Id: rs1783919992

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130472del , CM000668.2:g.18130472del	GRCh38
NC_000006.11:g.18130703del , CM000668.1:g.18130703del	GRCh37
NC_000006.10:g.18238682del	NCBI36
NG_012137.2:g.29675del
NG_012137.3:g.29675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.*199del MANE Select	ENSP00000312304.4:n.*199del
ENST00000309983.4:c.*199del	ENSP00000312304.4:n.*199del
NM_000367.3:c.*199del	NP_000358.1:n.*199del
XM_011514839.1:c.*199del	XP_011513141.1:n.*199del
XM_011514840.1:c.*199del	XP_011513142.1:n.*199del
NM_000367.4:c.*199del	NP_000358.1:n.*199del
NM_001346817.1:c.*199del	NP_001333746.1:n.*199del
NM_001346818.1:c.*199del	NP_001333747.1:n.*199del
NM_000367.5:c.*199del MANE Select	NP_000358.1:n.*199del