Canonical Allele Identifier: CA2839497121

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529405del , CM000684.2:g.50529405del	GRCh38
NC_000022.10:g.50967834del , CM000684.1:g.50967834del	GRCh37
NC_000022.9:g.49314700del	NCBI36
NG_011860.1:g.5682del , LRG_727:g.5682del
NG_016235.1:g.2036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.215-66del MANE Select	ENSP00000252029.3:n.215-66del
ENST00000395680.6:c.215-66del	ENSP00000379037.1:n.215-66del
ENST00000395681.6:c.215-66del	ENSP00000379038.1:n.215-66del
ENST00000650719.1:c.215-66del	ENSP00000498276.1:n.215-66del
ENST00000651095.1:n.354-66del
ENST00000651196.1:c.215-66del	ENSP00000499096.1:n.215-66del
ENST00000651401.1:c.-1+500del	ENSP00000499115.1:n.-1+500del
ENST00000651906.1:n.334-66del
ENST00000652237.1:n.425del
ENST00000252029.7:c.215-66del	ENSP00000252029.3:n.215-66del
ENST00000395678.7:c.215-66del	ENSP00000379036.3:n.215-66del
ENST00000395680.5:c.215-66del	ENSP00000379037.1:n.215-66del
ENST00000395681.5:c.215-66del	ENSP00000379038.1:n.215-66del
ENST00000425169.1:c.215-66del	ENSP00000395875.1:n.215-66del
ENST00000476284.1:n.340-66del
ENST00000487162.1:n.437del
ENST00000487577.5:n.502-66del
NM_001113755.2:c.215-66del	NP_001107227.1:n.215-66del
NM_001113756.2:c.215-66del	NP_001107228.1:n.215-66del
NM_001257988.1:c.215-66del , LRG_727t1:c.215-66del	NP_001244917.1:n.215-66del
NM_001257989.1:c.215-66del , LRG_727t2:c.215-66del	NP_001244918.1:n.215-66del
NM_001953.4:c.215-66del	NP_001944.1:n.215-66del
NM_001113755.3:c.215-66del	NP_001107227.1:n.215-66del
NM_001113756.3:c.215-66del	NP_001107228.1:n.215-66del
NM_001953.5:c.215-66del MANE Select	NP_001944.1:n.215-66del