Canonical Allele Identifier: CA2410909245

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50528561T= , CM000684.2:g.50528561T=	GRCh38
NC_000022.10:g.50966990T= , CM000684.1:g.50966990T=	GRCh37
NC_000022.9:g.49313856T=	NCBI36
NG_011860.1:g.6525A= , LRG_727:g.6525A=
NG_016235.1:g.2879A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001953.5:c.467A= MANE Select	NP_001944.1:p.Asp156=
ENST00000252029.8:c.467A= MANE Select	ENSP00000252029.3:p.Asp156=
NM_001113755.2:c.467A=	NP_001107227.1:p.Asp156=
NM_001113755.3:c.467A=	NP_001107227.1:p.Asp156=
NM_001113756.2:c.467A=	NP_001107228.1:p.Asp156=
NM_001113756.3:c.467A=	NP_001107228.1:p.Asp156=
NM_001257988.1:c.467A= , LRG_727t1:c.467A=	NP_001244917.1:p.Asp156=
NM_001257989.1:c.467A= , LRG_727t2:c.467A=	NP_001244918.1:p.Asp156=
NM_001953.4:c.467A=	NP_001944.1:p.Asp156=
ENST00000252029.7:c.467A=	ENSP00000252029.3:p.Asp156=
ENST00000395678.7:c.467A=	ENSP00000379036.3:p.Asp156=
ENST00000395680.5:c.467A=	ENSP00000379037.1:p.Asp156=
ENST00000395680.6:c.467A=	ENSP00000379037.1:p.Asp156=
ENST00000395681.5:c.467A=	ENSP00000379038.1:p.Asp156=
ENST00000395681.6:c.467A=	ENSP00000379038.1:p.Asp156=
ENST00000425169.1:c.417+575A=	ENSP00000395875.1:n.417+575A=
ENST00000476284.1:n.592A=
ENST00000487162.1:n.1280A=
ENST00000487577.5:n.754A=
ENST00000650719.1:c.467A=	ENSP00000498276.1:p.Asp156=
ENST00000651401.1:c.1-844A=	ENSP00000499115.1:n.1-844A=
ENST00000651906.1:n.586A=
ENST00000652352.1:c.178A=	ENSP00000498579.1:p.Ile60=