Canonical Allele Identifier: CA2410909238

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50528550A= , CM000684.2:g.50528550A=	GRCh38
NC_000022.10:g.50966979A= , CM000684.1:g.50966979A=	GRCh37
NC_000022.9:g.49313845A=	NCBI36
NG_011860.1:g.6536T= , LRG_727:g.6536T=
NG_016235.1:g.2890T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001953.5:c.478T= MANE Select	NP_001944.1:p.Ser160=
ENST00000252029.8:c.478T= MANE Select	ENSP00000252029.3:p.Ser160=
NM_001113755.2:c.478T=	NP_001107227.1:p.Ser160=
NM_001113755.3:c.478T=	NP_001107227.1:p.Ser160=
NM_001113756.2:c.478T=	NP_001107228.1:p.Ser160=
NM_001113756.3:c.478T=	NP_001107228.1:p.Ser160=
NM_001257988.1:c.478T= , LRG_727t1:c.478T=	NP_001244917.1:p.Ser160=
NM_001257989.1:c.478T= , LRG_727t2:c.478T=	NP_001244918.1:p.Ser160=
NM_001953.4:c.478T=	NP_001944.1:p.Ser160=
ENST00000252029.7:c.478T=	ENSP00000252029.3:p.Ser160=
ENST00000395678.7:c.478T=	ENSP00000379036.3:p.Ser160=
ENST00000395680.5:c.478T=	ENSP00000379037.1:p.Ser160=
ENST00000395680.6:c.478T=	ENSP00000379037.1:p.Ser160=
ENST00000395681.5:c.478T=	ENSP00000379038.1:p.Ser160=
ENST00000395681.6:c.478T=	ENSP00000379038.1:p.Ser160=
ENST00000425169.1:c.417+586T=	ENSP00000395875.1:n.417+586T=
ENST00000476284.1:n.603T=
ENST00000487162.1:n.1291T=
ENST00000487577.5:n.765T=
ENST00000650719.1:c.478T=	ENSP00000498276.1:p.Ser160=
ENST00000651401.1:c.1-833T=	ENSP00000499115.1:n.1-833T=
ENST00000651906.1:n.597T=
ENST00000652352.1:c.189T=	ENSP00000498579.1:p.Ser63=