Canonical Allele Identifier: CA2657566303

Gene: TYMP

Linked Data

• gnomAD v4: 22-50528656-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50528658_50528660del , CM000684.2:g.50528658_50528660del	GRCh38
NC_000022.10:g.50967087_50967089del , CM000684.1:g.50967087_50967089del	GRCh37
NC_000022.9:g.49313953_49313955del	NCBI36
NG_011860.1:g.6427_6429del , LRG_727:g.6427_6429del
NG_016235.1:g.2781_2783del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.418-49_418-47del MANE Select	ENSP00000252029.3:n.418-49_418-47del
ENST00000395680.6:c.418-49_418-47del	ENSP00000379037.1:n.418-49_418-47del
ENST00000395681.6:c.418-49_418-47del	ENSP00000379038.1:n.418-49_418-47del
ENST00000650719.1:c.418-49_418-47del	ENSP00000498276.1:n.418-49_418-47del
ENST00000651401.1:c.1-942_1-940del	ENSP00000499115.1:n.1-942_1-940del
ENST00000651906.1:n.537-49_537-47del
ENST00000652352.1:c.166-86_166-84del	ENSP00000498579.1:n.166-86_166-84del
ENST00000252029.7:c.418-49_418-47del	ENSP00000252029.3:n.418-49_418-47del
ENST00000395678.7:c.418-49_418-47del	ENSP00000379036.3:n.418-49_418-47del
ENST00000395680.5:c.418-49_418-47del	ENSP00000379037.1:n.418-49_418-47del
ENST00000395681.5:c.418-49_418-47del	ENSP00000379038.1:n.418-49_418-47del
ENST00000425169.1:c.417+477_417+479del	ENSP00000395875.1:n.417+477_417+479del
ENST00000476284.1:n.543-49_543-47del
ENST00000487162.1:n.1182_1184del
ENST00000487577.5:n.705-49_705-47del
NM_001113755.2:c.418-49_418-47del	NP_001107227.1:n.418-49_418-47del
NM_001113756.2:c.418-49_418-47del	NP_001107228.1:n.418-49_418-47del
NM_001257988.1:c.418-49_418-47del , LRG_727t1:c.418-49_418-47del	NP_001244917.1:n.418-49_418-47del
NM_001257989.1:c.418-49_418-47del , LRG_727t2:c.418-49_418-47del	NP_001244918.1:n.418-49_418-47del
NM_001953.4:c.418-49_418-47del	NP_001944.1:n.418-49_418-47del
NM_001113755.3:c.418-49_418-47del	NP_001107227.1:n.418-49_418-47del
NM_001113756.3:c.418-49_418-47del	NP_001107228.1:n.418-49_418-47del
NM_001953.5:c.418-49_418-47del MANE Select	NP_001944.1:n.418-49_418-47del