Canonical Allele Identifier: CA2695231069
Gene: TYMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50529338_50529351delinsTCACGC , CM000684.2:g.50529338_50529351delinsTCACGC GRCh38
NC_000022.10:g.50967767_50967780delinsTCACGC , CM000684.1:g.50967767_50967780delinsTCACGC GRCh37
NC_000022.9:g.49314633_49314646delinsTCACGC NCBI36
NG_011860.1:g.5735_5748delinsGCGTGA , LRG_727:g.5735_5748delinsGCGTGA
NG_016235.1:g.2089_2102delinsGCGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252029.8:c.215-13_215delinsGCGTGA
ENST00000395680.6:c.215-13_215delinsGCGTGA
ENST00000395681.6:c.215-13_215delinsGCGTGA
ENST00000650719.1:c.215-13_215delinsGCGTGA
ENST00000651095.1:n.354-13_354delinsGCGTGA
ENST00000651196.1:c.215-13_215delinsGCGTGA
ENST00000651401.1:c.-1+553_-1+566delinsGCGTGA ENSP00000499115.1:n.-1+553_-1+566delinsGCGTGA
ENST00000651906.1:n.334-13_334delinsGCGTGA
ENST00000652237.1:n.478_491delinsGCGTGA
ENST00000252029.7:c.215-13_215delinsGCGTGA
ENST00000395678.7:c.215-13_215delinsGCGTGA
ENST00000395680.5:c.215-13_215delinsGCGTGA
ENST00000395681.5:c.215-13_215delinsGCGTGA
ENST00000425169.1:c.215-13_215delinsGCGTGA
ENST00000476284.1:n.340-13_340delinsGCGTGA
ENST00000487162.1:n.490_503delinsGCGTGA
ENST00000487577.5:n.502-13_502delinsGCGTGA
NM_001113755.2:c.215-13_215delinsGCGTGA
NM_001113756.2:c.215-13_215delinsGCGTGA
NM_001257988.1:c.215-13_215delinsGCGTGA , LRG_727t1:c.215-13_215delinsGCGTGA
NM_001257989.1:c.215-13_215delinsGCGTGA , LRG_727t2:c.215-13_215delinsGCGTGA
NM_001953.4:c.215-13_215delinsGCGTGA
NM_001113755.3:c.215-13_215delinsGCGTGA
NM_001113756.3:c.215-13_215delinsGCGTGA
NM_001953.5:c.215-13_215delinsGCGTGA