Canonical Allele Identifier: CA2657567576
Gene: TYMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50529155dup , CM000684.2:g.50529155dup GRCh38
NC_000022.10:g.50967584dup , CM000684.1:g.50967584dup GRCh37
NC_000022.9:g.49314450dup NCBI36
NG_011860.1:g.5931dup , LRG_727:g.5931dup
NG_016235.1:g.2285dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252029.8:c.398dup MANE Select ENSP00000252029.3:p.Ala134GlyfsTer24
ENST00000395680.6:c.398dup ENSP00000379037.1:p.Ala134GlyfsTer24
ENST00000395681.6:c.398dup ENSP00000379038.1:p.Ala134GlyfsTer24
ENST00000650719.1:c.398dup ENSP00000498276.1:p.Ala134GlyfsTer24
ENST00000651095.1:n.537dup
ENST00000651196.1:c.398dup ENSP00000499096.1:p.Ala134GlyfsTer?
ENST00000651401.1:c.-1+749dup ENSP00000499115.1:n.-1+749dup
ENST00000651906.1:n.517dup
ENST00000652237.1:n.674dup
ENST00000652352.1:c.146dup ENSP00000498579.1:p.Ala50GlyfsTer?
ENST00000252029.7:c.398dup ENSP00000252029.3:p.Ala134GlyfsTer24
ENST00000395678.7:c.398dup ENSP00000379036.3:p.Ala134GlyfsTer24
ENST00000395680.5:c.398dup ENSP00000379037.1:p.Ala134GlyfsTer24
ENST00000395681.5:c.398dup ENSP00000379038.1:p.Ala134GlyfsTer24
ENST00000425169.1:c.398dup ENSP00000395875.1:p.Ala134GlyfsTer23
ENST00000476284.1:n.523dup
ENST00000487162.1:n.686dup
ENST00000487577.5:n.685dup
NM_001113755.2:c.398dup NP_001107227.1:p.Ala134GlyfsTer24
NM_001113756.2:c.398dup NP_001107228.1:p.Ala134GlyfsTer24
NM_001257988.1:c.398dup , LRG_727t1:c.398dup NP_001244917.1:p.Ala134GlyfsTer24
NM_001257989.1:c.398dup , LRG_727t2:c.398dup NP_001244918.1:p.Ala134GlyfsTer24
NM_001953.4:c.398dup NP_001944.1:p.Ala134GlyfsTer24
NM_001113755.3:c.398dup NP_001107227.1:p.Ala134GlyfsTer24
NM_001113756.3:c.398dup NP_001107228.1:p.Ala134GlyfsTer24
NM_001953.5:c.398dup MANE Select NP_001944.1:p.Ala134GlyfsTer24