Canonical Allele Identifier: CA1613565782

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18143805_18143806delinsTA , CM000668.2:g.18143805_18143806delinsTA	GRCh38
NC_000006.11:g.18144036_18144037delinsTA , CM000668.1:g.18144036_18144037delinsTA	GRCh37
NC_000006.10:g.18252015_18252016delinsTA	NCBI36
NG_012137.2:g.16338_16339delinsTA
NG_012137.3:g.16338_16339delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.234-78_234-77delinsTA MANE Select	ENSP00000312304.4:n.234-78_234-77delinsTA
ENST00000309983.4:c.234-78_234-77delinsTA	ENSP00000312304.4:n.234-78_234-77delinsTA
NM_000367.3:c.234-78_234-77delinsTA	NP_000358.1:n.234-78_234-77delinsTA
XM_011514839.1:c.234-78_234-77delinsTA	XP_011513141.1:n.234-78_234-77delinsTA
XM_011514840.1:c.165-78_165-77delinsTA	XP_011513142.1:n.165-78_165-77delinsTA
NM_000367.4:c.234-78_234-77delinsTA	NP_000358.1:n.234-78_234-77delinsTA
NM_001346817.1:c.234-78_234-77delinsTA	NP_001333746.1:n.234-78_234-77delinsTA
NM_001346818.1:c.234-78_234-77delinsTA	NP_001333747.1:n.234-78_234-77delinsTA
NM_000367.5:c.234-78_234-77delinsTA MANE Select	NP_000358.1:n.234-78_234-77delinsTA