Canonical Allele Identifier: CA2410909596

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529215A= , CM000684.2:g.50529215A=	GRCh38
NC_000022.10:g.50967644A= , CM000684.1:g.50967644A=	GRCh37
NC_000022.9:g.49314510A=	NCBI36
NG_011860.1:g.5871T= , LRG_727:g.5871T=
NG_016235.1:g.2225T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.338T= MANE Select	ENSP00000252029.3:p.Val113=
ENST00000395680.6:c.338T=	ENSP00000379037.1:p.Val113=
ENST00000395681.6:c.338T=	ENSP00000379038.1:p.Val113=
ENST00000650719.1:c.338T=	ENSP00000498276.1:p.Val113=
ENST00000651095.1:n.477T=
ENST00000651196.1:c.338T=	ENSP00000499096.1:p.Val113=
ENST00000651401.1:c.-1+689T=	ENSP00000499115.1:n.-1+689T=
ENST00000651906.1:n.457T=
ENST00000652237.1:n.614T=
ENST00000652352.1:c.86T=	ENSP00000498579.1:p.Val29=
ENST00000252029.7:c.338T=	ENSP00000252029.3:p.Val113=
ENST00000395678.7:c.338T=	ENSP00000379036.3:p.Val113=
ENST00000395680.5:c.338T=	ENSP00000379037.1:p.Val113=
ENST00000395681.5:c.338T=	ENSP00000379038.1:p.Val113=
ENST00000425169.1:c.338T=	ENSP00000395875.1:p.Val113=
ENST00000476284.1:n.463T=
ENST00000487162.1:n.626T=
ENST00000487577.5:n.625T=
NM_001113755.2:c.338T=	NP_001107227.1:p.Val113=
NM_001113756.2:c.338T=	NP_001107228.1:p.Val113=
NM_001257988.1:c.338T= , LRG_727t1:c.338T=	NP_001244917.1:p.Val113=
NM_001257989.1:c.338T= , LRG_727t2:c.338T=	NP_001244918.1:p.Val113=
NM_001953.4:c.338T=	NP_001944.1:p.Val113=
NM_001113755.3:c.338T=	NP_001107227.1:p.Val113=
NM_001113756.3:c.338T=	NP_001107228.1:p.Val113=
NM_001953.5:c.338T= MANE Select	NP_001944.1:p.Val113=