Canonical Allele Identifier: CA1613558601

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18139516_18139519delinsTAAA , CM000668.2:g.18139516_18139519delinsTAAA	GRCh38
NC_000006.11:g.18139747_18139750delinsTAAA , CM000668.1:g.18139747_18139750delinsTAAA	GRCh37
NC_000006.10:g.18247726_18247729delinsTAAA	NCBI36
NG_012137.2:g.20625_20628delinsTTTA
NG_012137.3:g.20625_20628delinsTTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.419+146_419+149delinsTTTA MANE Select	ENSP00000312304.4:n.419+146_419+149delins...
ENST00000309983.4:c.419+146_419+149delinsTTTA	ENSP00000312304.4:n.419+146_419+149delins...
NM_000367.3:c.419+146_419+149delinsTTTA	NP_000358.1:n.419+146_419+149delinsTTTA
XM_011514839.1:c.419+146_419+149delinsTTTA	XP_011513141.1:n.419+146_419+149delinsTTT...
XM_011514840.1:c.350+146_350+149delinsTTTA	XP_011513142.1:n.350+146_350+149delinsTTT...
NM_000367.4:c.419+146_419+149delinsTTTA	NP_000358.1:n.419+146_419+149delinsTTTA
NM_001346817.1:c.419+146_419+149delinsTTTA	NP_001333746.1:n.419+146_419+149delinsTTT...
NM_001346818.1:c.419+146_419+149delinsTTTA	NP_001333747.1:n.419+146_419+149delinsTTT...
NM_000367.5:c.419+146_419+149delinsTTTA MANE Select	NP_000358.1:n.419+146_419+149delinsTTTA