Canonical Allele Identifier: CA2677457400
Gene: TPMT HGNC NCBI

Linked Data

gnomAD v4: 6-18138811-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.18138811C>A , CM000668.2:g.18138811C>A GRCh38
NC_000006.11:g.18139042C>A , CM000668.1:g.18139042C>A GRCh37
NC_000006.10:g.18247021C>A NCBI36
NG_012137.2:g.21333G>T
NG_012137.3:g.21333G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309983.5:c.494+152G>T MANE Select ENSP00000312304.4:n.494+152G>T
ENST00000309983.4:c.494+152G>T ENSP00000312304.4:n.494+152G>T
NM_000367.3:c.494+152G>T NP_000358.1:n.494+152G>T
XM_011514839.1:c.494+152G>T XP_011513141.1:n.494+152G>T
XM_011514840.1:c.425+152G>T XP_011513142.1:n.425+152G>T
NM_000367.4:c.494+152G>T NP_000358.1:n.494+152G>T
NM_001346817.1:c.494+152G>T NP_001333746.1:n.494+152G>T
NM_001346818.1:c.494+152G>T NP_001333747.1:n.494+152G>T
NM_000367.5:c.494+152G>T MANE Select NP_000358.1:n.494+152G>T