Canonical Allele Identifier: CA362838244
Gene: TPMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18143639G>A , CM000668.2:g.18143639G>A GRCh38
NC_000006.11:g.18143870G>A , CM000668.1:g.18143870G>A GRCh37
NC_000006.10:g.18251849G>A NCBI36
NG_012137.2:g.16505C>T
NG_012137.3:g.16505C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.323C>T MANE Select ENSP00000312304.4:p.Ser108Leu
ENST00000309983.4:c.323C>T ENSP00000312304.4:p.Ser108Leu
NM_000367.3:c.323C>T NP_000358.1:p.Ser108Leu
XM_011514839.1:c.323C>T XP_011513141.1:p.Ser108Leu
XM_011514840.1:c.254C>T XP_011513142.1:p.Ser85Leu
NM_000367.4:c.323C>T NP_000358.1:p.Ser108Leu
NM_001346817.1:c.323C>T NP_001333746.1:p.Ser108Leu
NM_001346818.1:c.323C>T NP_001333747.1:p.Ser108Leu
NM_000367.5:c.323C>T MANE Select NP_000358.1:p.Ser108Leu