Canonical Allele Identifier: CA1613558488

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18139437_18139438delinsTC , CM000668.2:g.18139437_18139438delinsTC	GRCh38
NC_000006.11:g.18139668_18139669delinsTC , CM000668.1:g.18139668_18139669delinsTC	GRCh37
NC_000006.10:g.18247647_18247648delinsTC	NCBI36
NG_012137.2:g.20706_20707delinsGA
NG_012137.3:g.20706_20707delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.419+227_419+228delinsGA MANE Select	ENSP00000312304.4:n.419+227_419+228delinsGA
ENST00000309983.4:c.419+227_419+228delinsGA	ENSP00000312304.4:n.419+227_419+228delinsGA
NM_000367.3:c.419+227_419+228delinsGA	NP_000358.1:n.419+227_419+228delinsGA
XM_011514839.1:c.419+227_419+228delinsGA	XP_011513141.1:n.419+227_419+228delinsGA
XM_011514840.1:c.350+227_350+228delinsGA	XP_011513142.1:n.350+227_350+228delinsGA
NM_000367.4:c.419+227_419+228delinsGA	NP_000358.1:n.419+227_419+228delinsGA
NM_001346817.1:c.419+227_419+228delinsGA	NP_001333746.1:n.419+227_419+228delinsGA
NM_001346818.1:c.419+227_419+228delinsGA	NP_001333747.1:n.419+227_419+228delinsGA
NM_000367.5:c.419+227_419+228delinsGA MANE Select	NP_000358.1:n.419+227_419+228delinsGA