Canonical Allele Identifier: CA1613565504

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18143703_18143704delinsCT , CM000668.2:g.18143703_18143704delinsCT	GRCh38
NC_000006.11:g.18143934_18143935delinsCT , CM000668.1:g.18143934_18143935delinsCT	GRCh37
NC_000006.10:g.18251913_18251914delinsCT	NCBI36
NG_012137.2:g.16440_16441delinsAG
NG_012137.3:g.16440_16441delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.258_259delinsAG MANE Select	ENSP00000312304.4:p.Val86=
ENST00000309983.4:c.258_259delinsAG	ENSP00000312304.4:p.Val86=
NM_000367.3:c.258_259delinsAG	NP_000358.1:p.Val86=
XM_011514839.1:c.258_259delinsAG	XP_011513141.1:p.Val86=
XM_011514840.1:c.189_190delinsAG	XP_011513142.1:p.Val63=
NM_000367.4:c.258_259delinsAG	NP_000358.1:p.Val86=
NM_001346817.1:c.258_259delinsAG	NP_001333746.1:p.Val86=
NM_001346818.1:c.258_259delinsAG	NP_001333747.1:p.Val86=
NM_000367.5:c.258_259delinsAG MANE Select	NP_000358.1:p.Val86=