Canonical Allele Identifier: CA2410908030

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526611C= , CM000684.2:g.50526611C=	GRCh38
NC_000022.10:g.50965040C= , CM000684.1:g.50965040C=	GRCh37
NC_000022.9:g.49311906C=	NCBI36
NG_011860.1:g.8475G= , LRG_727:g.8475G=
NG_016235.1:g.4829G=
NG_021419.1:g.23396C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001953.5:c.893G= MANE Select	NP_001944.1:p.Gly298=
ENST00000252029.8:c.893G= MANE Select	ENSP00000252029.3:p.Gly298=
NM_001113755.2:c.893G=	NP_001107227.1:p.Gly298=
NM_001113755.3:c.893G=	NP_001107227.1:p.Gly298=
NM_001113756.2:c.893G=	NP_001107228.1:p.Gly298=
NM_001113756.3:c.893G=	NP_001107228.1:p.Gly298=
NM_001257988.1:c.893G= , LRG_727t1:c.893G=	NP_001244917.1:p.Gly298=
NM_001257989.1:c.893G= , LRG_727t2:c.893G=	NP_001244918.1:p.Gly298=
NM_001953.4:c.893G=	NP_001944.1:p.Gly298=
ENST00000252029.7:c.893G=	ENSP00000252029.3:p.Gly298=
ENST00000395678.7:c.893G=	ENSP00000379036.3:p.Gly298=
ENST00000395680.5:c.893G=	ENSP00000379037.1:p.Gly298=
ENST00000395680.6:c.893G=	ENSP00000379037.1:p.Gly298=
ENST00000395681.5:c.893G=	ENSP00000379038.1:p.Gly298=
ENST00000395681.6:c.893G=	ENSP00000379038.1:p.Gly298=
ENST00000425169.1:c.794G=	ENSP00000395875.1:p.Gly265=
ENST00000476284.1:n.899G=
ENST00000487577.5:n.1180G=
ENST00000650719.1:c.774G=	ENSP00000498276.1:p.Arg258=
ENST00000651401.1:c.377G=	ENSP00000499115.1:p.Gly126=
ENST00000652401.1:c.394G=