Canonical Allele Identifier: CA362838334

Gene: TPMT

Linked Data

• MyVariant Identifiers: chr6:g.18143893A>T (hg19) ; chr6:g.18143662A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18143662A>T , CM000668.2:g.18143662A>T	GRCh38
NC_000006.11:g.18143893A>T , CM000668.1:g.18143893A>T	GRCh37
NC_000006.10:g.18251872A>T	NCBI36
NG_012137.2:g.16482T>A
NG_012137.3:g.16482T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.300T>A MANE Select	ENSP00000312304.4:p.Phe100Leu
ENST00000309983.4:c.300T>A	ENSP00000312304.4:p.Phe100Leu
NM_000367.3:c.300T>A	NP_000358.1:p.Phe100Leu
XM_011514839.1:c.300T>A	XP_011513141.1:p.Phe100Leu
XM_011514840.1:c.231T>A	XP_011513142.1:p.Phe77Leu
NM_000367.4:c.300T>A	NP_000358.1:p.Phe100Leu
NM_001346817.1:c.300T>A	NP_001333746.1:p.Phe100Leu
NM_001346818.1:c.300T>A	NP_001333747.1:p.Phe100Leu
NM_000367.5:c.300T>A MANE Select	NP_000358.1:p.Phe100Leu