Canonical Allele Identifier: CA515387873

Gene: TYMP

Linked Data

• ClinVar Variation Id: 1532838
• ClinVar RCV Id: RCV002087332
• dbSNP Id: rs759097455
• MyVariant Identifiers: chr22:g.50968121G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529692G>A , CM000684.2:g.50529692G>A	GRCh38
NC_000022.10:g.50968121G>A , CM000684.1:g.50968121G>A	GRCh37
NC_000022.9:g.49314987G>A	NCBI36
NG_011860.1:g.5394C>T , LRG_727:g.5394C>T
NG_016235.1:g.1748C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.18C>T MANE Select	ENSP00000252029.3:p.Thr6=
ENST00000395680.6:c.18C>T	ENSP00000379037.1:p.Thr6=
ENST00000395681.6:c.18C>T	ENSP00000379038.1:p.Thr6=
ENST00000650719.1:c.18C>T	ENSP00000498276.1:p.Thr6=
ENST00000651095.1:n.157C>T
ENST00000651196.1:c.18C>T	ENSP00000499096.1:p.Thr6=
ENST00000651401.1:c.-1+212C>T	ENSP00000499115.1:n.-1+212C>T
ENST00000651906.1:n.137C>T
ENST00000652237.1:n.137C>T
ENST00000252029.7:c.18C>T	ENSP00000252029.3:p.Thr6=
ENST00000395678.7:c.18C>T	ENSP00000379036.3:p.Thr6=
ENST00000395680.5:c.18C>T	ENSP00000379037.1:p.Thr6=
ENST00000395681.5:c.18C>T	ENSP00000379038.1:p.Thr6=
ENST00000425169.1:c.18C>T	ENSP00000395875.1:p.Thr6=
ENST00000476284.1:n.143C>T
ENST00000487162.1:n.149C>T
ENST00000487577.5:n.305C>T
NM_001113755.2:c.18C>T	NP_001107227.1:p.Thr6=
NM_001113756.2:c.18C>T	NP_001107228.1:p.Thr6=
NM_001257988.1:c.18C>T , LRG_727t1:c.18C>T	NP_001244917.1:p.Thr6=
NM_001257989.1:c.18C>T , LRG_727t2:c.18C>T	NP_001244918.1:p.Thr6=
NM_001953.4:c.18C>T	NP_001944.1:p.Thr6=
NM_001113755.3:c.18C>T	NP_001107227.1:p.Thr6=
NM_001113756.3:c.18C>T	NP_001107228.1:p.Thr6=
NM_001953.5:c.18C>T MANE Select	NP_001944.1:p.Thr6=