Canonical Allele Identifier: CA2410907990

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526560A= , CM000684.2:g.50526560A=	GRCh38
NC_000022.10:g.50964989A= , CM000684.1:g.50964989A=	GRCh37
NC_000022.9:g.49311855A=	NCBI36
NG_011860.1:g.8526T= , LRG_727:g.8526T=
NG_016235.1:g.4880T=
NG_021419.1:g.23345A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.928+16T= MANE Select	ENSP00000252029.3:n.928+16T=
ENST00000395680.6:c.928+16T=	ENSP00000379037.1:n.928+16T=
ENST00000395681.6:c.928+16T=	ENSP00000379038.1:n.928+16T=
ENST00000650719.1:c.809+16T=	ENSP00000498276.1:n.809+16T=
ENST00000651401.1:c.412+16T=	ENSP00000499115.1:n.412+16T=
ENST00000652401.1:c.429+16T=
ENST00000252029.7:c.928+16T=	ENSP00000252029.3:n.928+16T=
ENST00000395678.7:c.928+16T=	ENSP00000379036.3:n.928+16T=
ENST00000395680.5:c.928+16T=	ENSP00000379037.1:n.928+16T=
ENST00000395681.5:c.928+16T=	ENSP00000379038.1:n.928+16T=
ENST00000425169.1:c.829+16T=	ENSP00000395875.1:n.829+16T=
ENST00000476284.1:n.934+16T=
ENST00000487577.5:n.1215+16T=
NM_001113755.2:c.928+16T=	NP_001107227.1:n.928+16T=
NM_001113756.2:c.928+16T=	NP_001107228.1:n.928+16T=
NM_001257988.1:c.928+16T= , LRG_727t1:c.928+16T=	NP_001244917.1:n.928+16T=
NM_001257989.1:c.928+16T= , LRG_727t2:c.928+16T=	NP_001244918.1:n.928+16T=
NM_001953.4:c.928+16T=	NP_001944.1:n.928+16T=
NM_001113755.3:c.928+16T=	NP_001107227.1:n.928+16T=
NM_001113756.3:c.928+16T=	NP_001107228.1:n.928+16T=
NM_001953.5:c.928+16T= MANE Select	NP_001944.1:n.928+16T=