Canonical Allele Identifier: CA2410908065

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526660C= , CM000684.2:g.50526660C=	GRCh38
NC_000022.10:g.50965089C= , CM000684.1:g.50965089C=	GRCh37
NC_000022.9:g.49311955C=	NCBI36
NG_011860.1:g.8426G= , LRG_727:g.8426G=
NG_016235.1:g.4780G=
NG_021419.1:g.23445C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.844G= MANE Select	ENSP00000252029.3:p.Gly282=
ENST00000395680.6:c.844G=	ENSP00000379037.1:p.Gly282=
ENST00000395681.6:c.844G=	ENSP00000379038.1:p.Gly282=
ENST00000650719.1:c.725G=	ENSP00000498276.1:p.Gly242=
ENST00000651401.1:c.328G=	ENSP00000499115.1:p.Gly110=
ENST00000652401.1:c.345G=
ENST00000252029.7:c.844G=	ENSP00000252029.3:p.Gly282=
ENST00000395678.7:c.844G=	ENSP00000379036.3:p.Gly282=
ENST00000395680.5:c.844G=	ENSP00000379037.1:p.Gly282=
ENST00000395681.5:c.844G=	ENSP00000379038.1:p.Gly282=
ENST00000425169.1:c.745G=	ENSP00000395875.1:p.Gly249=
ENST00000476284.1:n.850G=
ENST00000487577.5:n.1131G=
NM_001113755.2:c.844G=	NP_001107227.1:p.Gly282=
NM_001113756.2:c.844G=	NP_001107228.1:p.Gly282=
NM_001257988.1:c.844G= , LRG_727t1:c.844G=	NP_001244917.1:p.Gly282=
NM_001257989.1:c.844G= , LRG_727t2:c.844G=	NP_001244918.1:p.Gly282=
NM_001953.4:c.844G=	NP_001944.1:p.Gly282=
NM_001113755.3:c.844G=	NP_001107227.1:p.Gly282=
NM_001113756.3:c.844G=	NP_001107228.1:p.Gly282=
NM_001953.5:c.844G= MANE Select	NP_001944.1:p.Gly282=