Canonical Allele Identifier: CA515387713
Gene: TYMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50967941C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50529512C>G , CM000684.2:g.50529512C>G GRCh38
NC_000022.10:g.50967941C>G , CM000684.1:g.50967941C>G GRCh37
NC_000022.9:g.49314807C>G NCBI36
NG_011860.1:g.5574G>C , LRG_727:g.5574G>C
NG_016235.1:g.1928G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.198G>C MANE Select ENSP00000252029.3:p.Ala66=
ENST00000395680.6:c.198G>C ENSP00000379037.1:p.Ala66=
ENST00000395681.6:c.198G>C ENSP00000379038.1:p.Ala66=
ENST00000650719.1:c.198G>C ENSP00000498276.1:p.Ala66=
ENST00000651095.1:n.337G>C
ENST00000651196.1:c.198G>C ENSP00000499096.1:p.Ala66=
ENST00000651401.1:c.-1+392G>C ENSP00000499115.1:n.-1+392G>C
ENST00000651906.1:n.317G>C
ENST00000652237.1:n.317G>C
ENST00000252029.7:c.198G>C ENSP00000252029.3:p.Ala66=
ENST00000395678.7:c.198G>C ENSP00000379036.3:p.Ala66=
ENST00000395680.5:c.198G>C ENSP00000379037.1:p.Ala66=
ENST00000395681.5:c.198G>C ENSP00000379038.1:p.Ala66=
ENST00000425169.1:c.198G>C ENSP00000395875.1:p.Ala66=
ENST00000476284.1:n.323G>C
ENST00000487162.1:n.329G>C
ENST00000487577.5:n.485G>C
NM_001113755.2:c.198G>C NP_001107227.1:p.Ala66=
NM_001113756.2:c.198G>C NP_001107228.1:p.Ala66=
NM_001257988.1:c.198G>C , LRG_727t1:c.198G>C NP_001244917.1:p.Ala66=
NM_001257989.1:c.198G>C , LRG_727t2:c.198G>C NP_001244918.1:p.Ala66=
NM_001953.4:c.198G>C NP_001944.1:p.Ala66=
NM_001113755.3:c.198G>C NP_001107227.1:p.Ala66=
NM_001113756.3:c.198G>C NP_001107228.1:p.Ala66=
NM_001953.5:c.198G>C MANE Select NP_001944.1:p.Ala66=