Canonical Allele Identifier: CA515387660

Gene: TYMP

Linked Data

• ClinVar Variation Id: 1121589
• ClinVar RCV Id: RCV001451895
• dbSNP Id: rs756488096
• gnomAD v2: 22-50968049-C-A
• gnomAD v3: 22-50529620-C-A
• gnomAD v4: 22-50529620-C-A
• MyVariant Identifiers: chr22:g.50968049C>A (hg19) ; chr22:g.50529620C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529620C>A , CM000684.2:g.50529620C>A	GRCh38
NC_000022.10:g.50968049C>A , CM000684.1:g.50968049C>A	GRCh37
NC_000022.9:g.49314915C>A	NCBI36
NG_011860.1:g.5466G>T , LRG_727:g.5466G>T
NG_016235.1:g.1820G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.90G>T MANE Select	ENSP00000252029.3:p.Ser30=
ENST00000395680.6:c.90G>T	ENSP00000379037.1:p.Ser30=
ENST00000395681.6:c.90G>T	ENSP00000379038.1:p.Ser30=
ENST00000650719.1:c.90G>T	ENSP00000498276.1:p.Ser30=
ENST00000651095.1:n.229G>T
ENST00000651196.1:c.90G>T	ENSP00000499096.1:p.Ser30=
ENST00000651401.1:c.-1+284G>T	ENSP00000499115.1:n.-1+284G>T
ENST00000651906.1:n.209G>T
ENST00000652237.1:n.209G>T
ENST00000252029.7:c.90G>T	ENSP00000252029.3:p.Ser30=
ENST00000395678.7:c.90G>T	ENSP00000379036.3:p.Ser30=
ENST00000395680.5:c.90G>T	ENSP00000379037.1:p.Ser30=
ENST00000395681.5:c.90G>T	ENSP00000379038.1:p.Ser30=
ENST00000425169.1:c.90G>T	ENSP00000395875.1:p.Ser30=
ENST00000476284.1:n.215G>T
ENST00000487162.1:n.221G>T
ENST00000487577.5:n.377G>T
NM_001113755.2:c.90G>T	NP_001107227.1:p.Ser30=
NM_001113756.2:c.90G>T	NP_001107228.1:p.Ser30=
NM_001257988.1:c.90G>T , LRG_727t1:c.90G>T	NP_001244917.1:p.Ser30=
NM_001257989.1:c.90G>T , LRG_727t2:c.90G>T	NP_001244918.1:p.Ser30=
NM_001953.4:c.90G>T	NP_001944.1:p.Ser30=
NM_001113755.3:c.90G>T	NP_001107227.1:p.Ser30=
NM_001113756.3:c.90G>T	NP_001107228.1:p.Ser30=
NM_001953.5:c.90G>T MANE Select	NP_001944.1:p.Ser30=