Canonical Allele Identifier: CA2819314696

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50527557_50527561del , CM000684.2:g.50527557_50527561del	GRCh38
NC_000022.10:g.50965986_50965990del , CM000684.1:g.50965986_50965990del	GRCh37
NC_000022.9:g.49312852_49312856del	NCBI36
NG_011860.1:g.7525_7529del , LRG_727:g.7525_7529del
NG_016235.1:g.3879_3883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.646+27_646+31del MANE Select	ENSP00000252029.3:n.646+27_646+31del
ENST00000395680.6:c.646+27_646+31del	ENSP00000379037.1:n.646+27_646+31del
ENST00000395681.6:c.646+27_646+31del	ENSP00000379038.1:n.646+27_646+31del
ENST00000650719.1:c.646+27_646+31del	ENSP00000498276.1:n.646+27_646+31del
ENST00000651401.1:c.130+27_130+31del	ENSP00000499115.1:n.130+27_130+31del
ENST00000651906.1:n.792_796del
ENST00000652352.1:c.357+27_357+31del	ENSP00000498579.1:n.357+27_357+31del
ENST00000652401.1:c.102+27_102+31del
ENST00000252029.7:c.646+27_646+31del	ENSP00000252029.3:n.646+27_646+31del
ENST00000395678.7:c.646+27_646+31del	ENSP00000379036.3:n.646+27_646+31del
ENST00000395680.5:c.646+27_646+31del	ENSP00000379037.1:n.646+27_646+31del
ENST00000395681.5:c.646+27_646+31del	ENSP00000379038.1:n.646+27_646+31del
ENST00000425169.1:c.547+27_547+31del	ENSP00000395875.1:n.547+27_547+31del
ENST00000476284.1:n.771+27_771+31del
ENST00000487577.5:n.933+27_933+31del
NM_001113755.2:c.646+27_646+31del	NP_001107227.1:n.646+27_646+31del
NM_001113756.2:c.646+27_646+31del	NP_001107228.1:n.646+27_646+31del
NM_001257988.1:c.646+27_646+31del , LRG_727t1:c.646+27_646+31del	NP_001244917.1:n.646+27_646+31del
NM_001257989.1:c.646+27_646+31del , LRG_727t2:c.646+27_646+31del	NP_001244918.1:n.646+27_646+31del
NM_001953.4:c.646+27_646+31del	NP_001944.1:n.646+27_646+31del
NM_001113755.3:c.646+27_646+31del	NP_001107227.1:n.646+27_646+31del
NM_001113756.3:c.646+27_646+31del	NP_001107228.1:n.646+27_646+31del
NM_001953.5:c.646+27_646+31del MANE Select	NP_001944.1:n.646+27_646+31del