Canonical Allele Identifier: CA1613545582
Gene: TPMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18130561G= , CM000668.2:g.18130561G= GRCh38
NC_000006.11:g.18130792G= , CM000668.1:g.18130792G= GRCh37
NC_000006.10:g.18238771G= NCBI36
NG_012137.2:g.29583C=
NG_012137.3:g.29583C=

Transcript Alleles

HGVS Amino-acid change
ENST00000309983.5:c.*107C= MANE Select ENSP00000312304.4:n.*107C=
ENST00000309983.4:c.*107C= ENSP00000312304.4:n.*107C=
NM_000367.3:c.*107C= NP_000358.1:n.*107C=
XM_011514839.1:c.*107C= XP_011513141.1:n.*107C=
XM_011514840.1:c.*107C= XP_011513142.1:n.*107C=
NM_000367.4:c.*107C= NP_000358.1:n.*107C=
NM_001346817.1:c.*107C= NP_001333746.1:n.*107C=
NM_001346818.1:c.*107C= NP_001333747.1:n.*107C=
NM_000367.5:c.*107C= MANE Select NP_000358.1:n.*107C=