Canonical Allele Identifier: CA412201920

Gene: TYMP

Linked Data

• dbSNP Id: rs1443174984
• gnomAD v2: 22-50967573-C-T
• gnomAD v3: 22-50529144-C-T
• gnomAD v4: 22-50529144-C-T
• MyVariant Identifiers: chr22:g.50967573C>T (hg19) ; chr22:g.50529144C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529144C>T , CM000684.2:g.50529144C>T	GRCh38
NC_000022.10:g.50967573C>T , CM000684.1:g.50967573C>T	GRCh37
NC_000022.9:g.49314439C>T	NCBI36
NG_011860.1:g.5942G>A , LRG_727:g.5942G>A
NG_016235.1:g.2296G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.409G>A MANE Select	ENSP00000252029.3:p.Gly137Ser
ENST00000395680.6:c.409G>A	ENSP00000379037.1:p.Gly137Ser
ENST00000395681.6:c.409G>A	ENSP00000379038.1:p.Gly137Ser
ENST00000650719.1:c.409G>A	ENSP00000498276.1:p.Gly137Ser
ENST00000651095.1:n.548G>A
ENST00000651196.1:c.409G>A	ENSP00000499096.1:p.Gly137Ser
ENST00000651401.1:c.-1+760G>A	ENSP00000499115.1:n.-1+760G>A
ENST00000651906.1:n.528G>A
ENST00000652237.1:n.685G>A
ENST00000652352.1:c.157G>A	ENSP00000498579.1:p.Gly53Ser
ENST00000252029.7:c.409G>A	ENSP00000252029.3:p.Gly137Ser
ENST00000395678.7:c.409G>A	ENSP00000379036.3:p.Gly137Ser
ENST00000395680.5:c.409G>A	ENSP00000379037.1:p.Gly137Ser
ENST00000395681.5:c.409G>A	ENSP00000379038.1:p.Gly137Ser
ENST00000425169.1:c.409G>A	ENSP00000395875.1:p.Gly137Ser
ENST00000476284.1:n.534G>A
ENST00000487162.1:n.697G>A
ENST00000487577.5:n.696G>A
NM_001113755.2:c.409G>A	NP_001107227.1:p.Gly137Ser
NM_001113756.2:c.409G>A	NP_001107228.1:p.Gly137Ser
NM_001257988.1:c.409G>A , LRG_727t1:c.409G>A	NP_001244917.1:p.Gly137Ser
NM_001257989.1:c.409G>A , LRG_727t2:c.409G>A	NP_001244918.1:p.Gly137Ser
NM_001953.4:c.409G>A	NP_001944.1:p.Gly137Ser
NM_001113755.3:c.409G>A	NP_001107227.1:p.Gly137Ser
NM_001113756.3:c.409G>A	NP_001107228.1:p.Gly137Ser
NM_001953.5:c.409G>A MANE Select	NP_001944.1:p.Gly137Ser