Canonical Allele Identifier: CA10321760

Gene: TYMP

Linked Data

• dbSNP Id: rs771977939
• ExAC: 22:50967086 C / T
• gnomAD v2: 22-50967086-C-T
• gnomAD v4: 22-50528657-C-T
• MyVariant Identifiers: chr22:g.50967086C>T (hg19) ; chr22:g.50528657C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50528657C>T , CM000684.2:g.50528657C>T	GRCh38
NC_000022.10:g.50967086C>T , CM000684.1:g.50967086C>T	GRCh37
NC_000022.9:g.49313952C>T	NCBI36
NG_011860.1:g.6429G>A , LRG_727:g.6429G>A
NG_016235.1:g.2783G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.418-47G>A MANE Select	ENSP00000252029.3:n.418-47G>A
ENST00000395680.6:c.418-47G>A	ENSP00000379037.1:n.418-47G>A
ENST00000395681.6:c.418-47G>A	ENSP00000379038.1:n.418-47G>A
ENST00000650719.1:c.418-47G>A	ENSP00000498276.1:n.418-47G>A
ENST00000651401.1:c.1-940G>A	ENSP00000499115.1:n.1-940G>A
ENST00000651906.1:n.537-47G>A
ENST00000652352.1:c.166-84G>A	ENSP00000498579.1:n.166-84G>A
ENST00000252029.7:c.418-47G>A	ENSP00000252029.3:n.418-47G>A
ENST00000395678.7:c.418-47G>A	ENSP00000379036.3:n.418-47G>A
ENST00000395680.5:c.418-47G>A	ENSP00000379037.1:n.418-47G>A
ENST00000395681.5:c.418-47G>A	ENSP00000379038.1:n.418-47G>A
ENST00000425169.1:c.417+479G>A	ENSP00000395875.1:n.417+479G>A
ENST00000476284.1:n.543-47G>A
ENST00000487162.1:n.1184G>A
ENST00000487577.5:n.705-47G>A
NM_001113755.2:c.418-47G>A	NP_001107227.1:n.418-47G>A
NM_001113756.2:c.418-47G>A	NP_001107228.1:n.418-47G>A
NM_001257988.1:c.418-47G>A , LRG_727t1:c.418-47G>A	NP_001244917.1:n.418-47G>A
NM_001257989.1:c.418-47G>A , LRG_727t2:c.418-47G>A	NP_001244918.1:n.418-47G>A
NM_001953.4:c.418-47G>A	NP_001944.1:n.418-47G>A
NM_001113755.3:c.418-47G>A	NP_001107227.1:n.418-47G>A
NM_001113756.3:c.418-47G>A	NP_001107228.1:n.418-47G>A
NM_001953.5:c.418-47G>A MANE Select	NP_001944.1:n.418-47G>A