Canonical Allele Identifier: CA1613558654

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18139556_18139557delinsTG , CM000668.2:g.18139556_18139557delinsTG	GRCh38
NC_000006.11:g.18139787_18139788delinsTG , CM000668.1:g.18139787_18139788delinsTG	GRCh37
NC_000006.10:g.18247766_18247767delinsTG	NCBI36
NG_012137.2:g.20587_20588delinsCA
NG_012137.3:g.20587_20588delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.419+108_419+109delinsCA MANE Select	ENSP00000312304.4:n.419+108_419+109delinsCA
ENST00000309983.4:c.419+108_419+109delinsCA	ENSP00000312304.4:n.419+108_419+109delinsCA
NM_000367.3:c.419+108_419+109delinsCA	NP_000358.1:n.419+108_419+109delinsCA
XM_011514839.1:c.419+108_419+109delinsCA	XP_011513141.1:n.419+108_419+109delinsCA
XM_011514840.1:c.350+108_350+109delinsCA	XP_011513142.1:n.350+108_350+109delinsCA
NM_000367.4:c.419+108_419+109delinsCA	NP_000358.1:n.419+108_419+109delinsCA
NM_001346817.1:c.419+108_419+109delinsCA	NP_001333746.1:n.419+108_419+109delinsCA
NM_001346818.1:c.419+108_419+109delinsCA	NP_001333747.1:n.419+108_419+109delinsCA
NM_000367.5:c.419+108_419+109delinsCA MANE Select	NP_000358.1:n.419+108_419+109delinsCA