Canonical Allele Identifier: CA1026670371
Gene: TYMP HGNC NCBI

Linked Data

dbSNP Id: rs2069437738

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50527528_50527532del , CM000684.2:g.50527528_50527532del GRCh38
NC_000022.10:g.50965957_50965961del , CM000684.1:g.50965957_50965961del GRCh37
NC_000022.9:g.49312823_49312827del NCBI36
NG_011860.1:g.7559_7563del , LRG_727:g.7559_7563del
NG_016235.1:g.3913_3917del

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.646+61_646+65del MANE Select ENSP00000252029.3:n.646+61_646+65del
ENST00000395680.6:c.646+61_646+65del ENSP00000379037.1:n.646+61_646+65del
ENST00000395681.6:c.646+61_646+65del ENSP00000379038.1:n.646+61_646+65del
ENST00000650719.1:c.646+61_646+65del ENSP00000498276.1:n.646+61_646+65del
ENST00000651401.1:c.130+61_130+65del ENSP00000499115.1:n.130+61_130+65del
ENST00000651906.1:n.826_830del
ENST00000652352.1:c.357+61_357+65del ENSP00000498579.1:n.357+61_357+65del
ENST00000652401.1:c.102+61_102+65del
ENST00000252029.7:c.646+61_646+65del ENSP00000252029.3:n.646+61_646+65del
ENST00000395678.7:c.646+61_646+65del ENSP00000379036.3:n.646+61_646+65del
ENST00000395680.5:c.646+61_646+65del ENSP00000379037.1:n.646+61_646+65del
ENST00000395681.5:c.646+61_646+65del ENSP00000379038.1:n.646+61_646+65del
ENST00000425169.1:c.547+61_547+65del ENSP00000395875.1:n.547+61_547+65del
ENST00000476284.1:n.771+61_771+65del
ENST00000487577.5:n.933+61_933+65del
NM_001113755.2:c.646+61_646+65del NP_001107227.1:n.646+61_646+65del
NM_001113756.2:c.646+61_646+65del NP_001107228.1:n.646+61_646+65del
NM_001257988.1:c.646+61_646+65del , LRG_727t1:c.646+61_646+65del NP_001244917.1:n.646+61_646+65del
NM_001257989.1:c.646+61_646+65del , LRG_727t2:c.646+61_646+65del NP_001244918.1:n.646+61_646+65del
NM_001953.4:c.646+61_646+65del NP_001944.1:n.646+61_646+65del
NM_001113755.3:c.646+61_646+65del NP_001107227.1:n.646+61_646+65del
NM_001113756.3:c.646+61_646+65del NP_001107228.1:n.646+61_646+65del
NM_001953.5:c.646+61_646+65del MANE Select NP_001944.1:n.646+61_646+65del