Canonical Allele Identifier: CA412202325

Gene: TYMP

Linked Data

• ClinVar Variation Id: 1972934
• ClinVar RCV Id: RCV002730895
• MyVariant Identifiers: chr22:g.50967748G>C (hg19) ; chr22:g.50529319G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529319G>C , CM000684.2:g.50529319G>C	GRCh38
NC_000022.10:g.50967748G>C , CM000684.1:g.50967748G>C	GRCh37
NC_000022.9:g.49314614G>C	NCBI36
NG_011860.1:g.5767C>G , LRG_727:g.5767C>G
NG_016235.1:g.2121C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.234C>G MANE Select	ENSP00000252029.3:p.Ile78Met
ENST00000395680.6:c.234C>G	ENSP00000379037.1:p.Ile78Met
ENST00000395681.6:c.234C>G	ENSP00000379038.1:p.Ile78Met
ENST00000650719.1:c.234C>G	ENSP00000498276.1:p.Ile78Met
ENST00000651095.1:n.373C>G
ENST00000651196.1:c.234C>G	ENSP00000499096.1:p.Ile78Met
ENST00000651401.1:c.-1+585C>G	ENSP00000499115.1:n.-1+585C>G
ENST00000651906.1:n.353C>G
ENST00000652237.1:n.510C>G
ENST00000252029.7:c.234C>G	ENSP00000252029.3:p.Ile78Met
ENST00000395678.7:c.234C>G	ENSP00000379036.3:p.Ile78Met
ENST00000395680.5:c.234C>G	ENSP00000379037.1:p.Ile78Met
ENST00000395681.5:c.234C>G	ENSP00000379038.1:p.Ile78Met
ENST00000425169.1:c.234C>G	ENSP00000395875.1:p.Ile78Met
ENST00000476284.1:n.359C>G
ENST00000487162.1:n.522C>G
ENST00000487577.5:n.521C>G
NM_001113755.2:c.234C>G	NP_001107227.1:p.Ile78Met
NM_001113756.2:c.234C>G	NP_001107228.1:p.Ile78Met
NM_001257988.1:c.234C>G , LRG_727t1:c.234C>G	NP_001244917.1:p.Ile78Met
NM_001257989.1:c.234C>G , LRG_727t2:c.234C>G	NP_001244918.1:p.Ile78Met
NM_001953.4:c.234C>G	NP_001944.1:p.Ile78Met
NM_001113755.3:c.234C>G	NP_001107227.1:p.Ile78Met
NM_001113756.3:c.234C>G	NP_001107228.1:p.Ile78Met
NM_001953.5:c.234C>G MANE Select	NP_001944.1:p.Ile78Met