Canonical Allele Identifier: CA2410908634

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50527535T= , CM000684.2:g.50527535T=	GRCh38
NC_000022.10:g.50965964T= , CM000684.1:g.50965964T=	GRCh37
NC_000022.9:g.49312830T=	NCBI36
NG_011860.1:g.7551A= , LRG_727:g.7551A=
NG_016235.1:g.3905A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.646+53A= MANE Select	ENSP00000252029.3:n.646+53A=
ENST00000395680.6:c.646+53A=	ENSP00000379037.1:n.646+53A=
ENST00000395681.6:c.646+53A=	ENSP00000379038.1:n.646+53A=
ENST00000650719.1:c.646+53A=	ENSP00000498276.1:n.646+53A=
ENST00000651401.1:c.130+53A=	ENSP00000499115.1:n.130+53A=
ENST00000651906.1:n.818A=
ENST00000652352.1:c.357+53A=	ENSP00000498579.1:n.357+53A=
ENST00000652401.1:c.102+53A=
ENST00000252029.7:c.646+53A=	ENSP00000252029.3:n.646+53A=
ENST00000395678.7:c.646+53A=	ENSP00000379036.3:n.646+53A=
ENST00000395680.5:c.646+53A=	ENSP00000379037.1:n.646+53A=
ENST00000395681.5:c.646+53A=	ENSP00000379038.1:n.646+53A=
ENST00000425169.1:c.547+53A=	ENSP00000395875.1:n.547+53A=
ENST00000476284.1:n.771+53A=
ENST00000487577.5:n.933+53A=
NM_001113755.2:c.646+53A=	NP_001107227.1:n.646+53A=
NM_001113756.2:c.646+53A=	NP_001107228.1:n.646+53A=
NM_001257988.1:c.646+53A= , LRG_727t1:c.646+53A=	NP_001244917.1:n.646+53A=
NM_001257989.1:c.646+53A= , LRG_727t2:c.646+53A=	NP_001244918.1:n.646+53A=
NM_001953.4:c.646+53A=	NP_001944.1:n.646+53A=
NM_001113755.3:c.646+53A=	NP_001107227.1:n.646+53A=
NM_001113756.3:c.646+53A=	NP_001107228.1:n.646+53A=
NM_001953.5:c.646+53A= MANE Select	NP_001944.1:n.646+53A=