Canonical Allele Identifier: CA1613558563

Gene: TPMT

Linked Data

• dbSNP Id: rs1784101827

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18139486dup , CM000668.2:g.18139486dup	GRCh38
NC_000006.11:g.18139717dup , CM000668.1:g.18139717dup	GRCh37
NC_000006.10:g.18247696dup	NCBI36
NG_012137.2:g.20661dup
NG_012137.3:g.20661dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.419+182dup MANE Select	ENSP00000312304.4:n.419+182dup
ENST00000309983.4:c.419+182dup	ENSP00000312304.4:n.419+182dup
NM_000367.3:c.419+182dup	NP_000358.1:n.419+182dup
XM_011514839.1:c.419+182dup	XP_011513141.1:n.419+182dup
XM_011514840.1:c.350+182dup	XP_011513142.1:n.350+182dup
NM_000367.4:c.419+182dup	NP_000358.1:n.419+182dup
NM_001346817.1:c.419+182dup	NP_001333746.1:n.419+182dup
NM_001346818.1:c.419+182dup	NP_001333747.1:n.419+182dup
NM_000367.5:c.419+182dup MANE Select	NP_000358.1:n.419+182dup