Canonical Allele Identifier: CA412199118

Gene: TYMP

Linked Data

• gnomAD v4: 22-50526660-C-A
• MyVariant Identifiers: chr22:g.50965089C>A (hg19) ; chr22:g.50526660C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526660C>A , CM000684.2:g.50526660C>A	GRCh38
NC_000022.10:g.50965089C>A , CM000684.1:g.50965089C>A	GRCh37
NC_000022.9:g.49311955C>A	NCBI36
NG_011860.1:g.8426G>T , LRG_727:g.8426G>T
NG_016235.1:g.4780G>T
NG_021419.1:g.23445C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.844G>T MANE Select	ENSP00000252029.3:p.Gly282Cys
ENST00000395680.6:c.844G>T	ENSP00000379037.1:p.Gly282Cys
ENST00000395681.6:c.844G>T	ENSP00000379038.1:p.Gly282Cys
ENST00000650719.1:c.725G>T	ENSP00000498276.1:p.Gly242Val
ENST00000651401.1:c.328G>T	ENSP00000499115.1:p.Gly110Cys
ENST00000652401.1:c.345G>T
ENST00000252029.7:c.844G>T	ENSP00000252029.3:p.Gly282Cys
ENST00000395678.7:c.844G>T	ENSP00000379036.3:p.Gly282Cys
ENST00000395680.5:c.844G>T	ENSP00000379037.1:p.Gly282Cys
ENST00000395681.5:c.844G>T	ENSP00000379038.1:p.Gly282Cys
ENST00000425169.1:c.745G>T	ENSP00000395875.1:p.Gly249Cys
ENST00000476284.1:n.850G>T
ENST00000487577.5:n.1131G>T
NM_001113755.2:c.844G>T	NP_001107227.1:p.Gly282Cys
NM_001113756.2:c.844G>T	NP_001107228.1:p.Gly282Cys
NM_001257988.1:c.844G>T , LRG_727t1:c.844G>T	NP_001244917.1:p.Gly282Cys
NM_001257989.1:c.844G>T , LRG_727t2:c.844G>T	NP_001244918.1:p.Gly282Cys
NM_001953.4:c.844G>T	NP_001944.1:p.Gly282Cys
NM_001113755.3:c.844G>T	NP_001107227.1:p.Gly282Cys
NM_001113756.3:c.844G>T	NP_001107228.1:p.Gly282Cys
NM_001953.5:c.844G>T MANE Select	NP_001944.1:p.Gly282Cys