Canonical Allele Identifier: CA565554995
Gene: TPMT HGNC NCBI

Linked Data

dbSNP Id: rs1415070928

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130542dup , CM000668.2:g.18130542dup GRCh38
NC_000006.11:g.18130773dup , CM000668.1:g.18130773dup GRCh37
NC_000006.10:g.18238752dup NCBI36
NG_012137.2:g.29606dup
NG_012137.3:g.29606dup

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*130dup MANE Select ENSP00000312304.4:n.*130dup
ENST00000309983.4:c.*130dup ENSP00000312304.4:n.*130dup
NM_000367.3:c.*130dup NP_000358.1:n.*130dup
XM_011514839.1:c.*130dup XP_011513141.1:n.*130dup
XM_011514840.1:c.*130dup XP_011513142.1:n.*130dup
NM_000367.4:c.*130dup NP_000358.1:n.*130dup
NM_001346817.1:c.*130dup NP_001333746.1:n.*130dup
NM_001346818.1:c.*130dup NP_001333747.1:n.*130dup
NM_000367.5:c.*130dup MANE Select NP_000358.1:n.*130dup