Canonical Allele Identifier: CA2410909563

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529149_50529150delinsGC , CM000684.2:g.50529149_50529150delinsGC	GRCh38
NC_000022.10:g.50967578_50967579delinsGC , CM000684.1:g.50967578_50967579delinsGC	GRCh37
NC_000022.9:g.49314444_49314445delinsGC	NCBI36
NG_011860.1:g.5936_5937delinsGC , LRG_727:g.5936_5937delinsGC
NG_016235.1:g.2290_2291delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.403_404delinsGC MANE Select	ENSP00000252029.3:p.Ala135=
ENST00000395680.6:c.403_404delinsGC	ENSP00000379037.1:p.Ala135=
ENST00000395681.6:c.403_404delinsGC	ENSP00000379038.1:p.Ala135=
ENST00000650719.1:c.403_404delinsGC	ENSP00000498276.1:p.Ala135=
ENST00000651095.1:n.542_543delinsGC
ENST00000651196.1:c.403_404delinsGC	ENSP00000499096.1:p.Ala135=
ENST00000651401.1:c.-1+754_-1+755delinsGC	ENSP00000499115.1:n.-1+754_-1+755delinsGC
ENST00000651906.1:n.522_523delinsGC
ENST00000652237.1:n.679_680delinsGC
ENST00000652352.1:c.151_152delinsGC	ENSP00000498579.1:p.Ala51=
ENST00000252029.7:c.403_404delinsGC	ENSP00000252029.3:p.Ala135=
ENST00000395678.7:c.403_404delinsGC	ENSP00000379036.3:p.Ala135=
ENST00000395680.5:c.403_404delinsGC	ENSP00000379037.1:p.Ala135=
ENST00000395681.5:c.403_404delinsGC	ENSP00000379038.1:p.Ala135=
ENST00000425169.1:c.403_404delinsGC	ENSP00000395875.1:p.Ala135=
ENST00000476284.1:n.528_529delinsGC
ENST00000487162.1:n.691_692delinsGC
ENST00000487577.5:n.690_691delinsGC
NM_001113755.2:c.403_404delinsGC	NP_001107227.1:p.Ala135=
NM_001113756.2:c.403_404delinsGC	NP_001107228.1:p.Ala135=
NM_001257988.1:c.403_404delinsGC , LRG_727t1:c.403_404delinsGC	NP_001244917.1:p.Ala135=
NM_001257989.1:c.403_404delinsGC , LRG_727t2:c.403_404delinsGC	NP_001244918.1:p.Ala135=
NM_001953.4:c.403_404delinsGC	NP_001944.1:p.Ala135=
NM_001113755.3:c.403_404delinsGC	NP_001107227.1:p.Ala135=
NM_001113756.3:c.403_404delinsGC	NP_001107228.1:p.Ala135=
NM_001953.5:c.403_404delinsGC MANE Select	NP_001944.1:p.Ala135=