Canonical Allele Identifier: CA1026669878

Gene: TYMP

Linked Data

• dbSNP Id: rs1165882750
• gnomAD v3: 22-50526767-C-T
• gnomAD v4: 22-50526767-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526767C>T , CM000684.2:g.50526767C>T	GRCh38
NC_000022.10:g.50965196C>T , CM000684.1:g.50965196C>T	GRCh37
NC_000022.9:g.49312062C>T	NCBI36
NG_011860.1:g.8319G>A , LRG_727:g.8319G>A
NG_016235.1:g.4673G>A
NG_021419.1:g.23552C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.766-29G>A MANE Select	ENSP00000252029.3:n.766-29G>A
ENST00000395680.6:c.766-29G>A	ENSP00000379037.1:n.766-29G>A
ENST00000395681.6:c.766-29G>A	ENSP00000379038.1:n.766-29G>A
ENST00000650719.1:c.647-29G>A	ENSP00000498276.1:n.647-29G>A
ENST00000651401.1:c.250-29G>A	ENSP00000499115.1:n.250-29G>A
ENST00000652352.1:c.477-29G>A	ENSP00000498579.1:n.477-29G>A
ENST00000652401.1:c.267-29G>A
ENST00000252029.7:c.766-29G>A	ENSP00000252029.3:n.766-29G>A
ENST00000395678.7:c.766-29G>A	ENSP00000379036.3:n.766-29G>A
ENST00000395680.5:c.766-29G>A	ENSP00000379037.1:n.766-29G>A
ENST00000395681.5:c.766-29G>A	ENSP00000379038.1:n.766-29G>A
ENST00000425169.1:c.667-29G>A	ENSP00000395875.1:n.667-29G>A
ENST00000476284.1:n.772-29G>A
ENST00000487577.5:n.1053-29G>A
NM_001113755.2:c.766-29G>A	NP_001107227.1:n.766-29G>A
NM_001113756.2:c.766-29G>A	NP_001107228.1:n.766-29G>A
NM_001257988.1:c.766-29G>A , LRG_727t1:c.766-29G>A	NP_001244917.1:n.766-29G>A
NM_001257989.1:c.766-29G>A , LRG_727t2:c.766-29G>A	NP_001244918.1:n.766-29G>A
NM_001953.4:c.766-29G>A	NP_001944.1:n.766-29G>A
NM_001113755.3:c.766-29G>A	NP_001107227.1:n.766-29G>A
NM_001113756.3:c.766-29G>A	NP_001107228.1:n.766-29G>A
NM_001953.5:c.766-29G>A MANE Select	NP_001944.1:n.766-29G>A