Canonical Allele Identifier: CA2591984088

Gene: TYMP

Linked Data

• gnomAD v3: 22-50529099-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529099G>A , CM000684.2:g.50529099G>A	GRCh38
NC_000022.10:g.50967528G>A , CM000684.1:g.50967528G>A	GRCh37
NC_000022.9:g.49314394G>A	NCBI36
NG_011860.1:g.5987C>T , LRG_727:g.5987C>T
NG_016235.1:g.2341C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.417+37C>T MANE Select	ENSP00000252029.3:n.417+37C>T
ENST00000395680.6:c.417+37C>T	ENSP00000379037.1:n.417+37C>T
ENST00000395681.6:c.417+37C>T	ENSP00000379038.1:n.417+37C>T
ENST00000650719.1:c.417+37C>T	ENSP00000498276.1:n.417+37C>T
ENST00000651095.1:n.593C>T
ENST00000651401.1:c.-1+805C>T	ENSP00000499115.1:n.-1+805C>T
ENST00000651906.1:n.536+37C>T
ENST00000652237.1:n.730C>T
ENST00000652352.1:c.165+37C>T	ENSP00000498579.1:n.165+37C>T
ENST00000252029.7:c.417+37C>T	ENSP00000252029.3:n.417+37C>T
ENST00000395678.7:c.417+37C>T	ENSP00000379036.3:n.417+37C>T
ENST00000395680.5:c.417+37C>T	ENSP00000379037.1:n.417+37C>T
ENST00000395681.5:c.417+37C>T	ENSP00000379038.1:n.417+37C>T
ENST00000425169.1:c.417+37C>T	ENSP00000395875.1:n.417+37C>T
ENST00000476284.1:n.542+37C>T
ENST00000487162.1:n.742C>T
ENST00000487577.5:n.704+37C>T
NM_001113755.2:c.417+37C>T	NP_001107227.1:n.417+37C>T
NM_001113756.2:c.417+37C>T	NP_001107228.1:n.417+37C>T
NM_001257988.1:c.417+37C>T , LRG_727t1:c.417+37C>T	NP_001244917.1:n.417+37C>T
NM_001257989.1:c.417+37C>T , LRG_727t2:c.417+37C>T	NP_001244918.1:n.417+37C>T
NM_001953.4:c.417+37C>T	NP_001944.1:n.417+37C>T
NM_001113755.3:c.417+37C>T	NP_001107227.1:n.417+37C>T
NM_001113756.3:c.417+37C>T	NP_001107228.1:n.417+37C>T
NM_001953.5:c.417+37C>T MANE Select	NP_001944.1:n.417+37C>T